Clinical Operations Jobs in Pharma & Biotech
88
Open Positions
13
Remote Jobs
75
With Salary Data
Clinical Operations professionals manage and execute clinical trials in pharmaceutical and biotech settings. These roles typically require experience in clinical research methodology and strong project management skills.
Key positions include:
- Clinical Research Associate (CRA)
- Clinical Trial Manager
- Clinical Operations Manager
- Clinical Study Coordinator
- Clinical Data Manager
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Job Posting Title PM CAL Coordinator IIFresh
Mar 21 Salary N/A Danvers, Massachusetts, United States of America Apply →Job Posting Title PM CAL Coordinator IIApply →Fresh
Mar 21 Salary N/A
Danvers, Massachusetts, United States of AmericaMakes key day-to-day contributions as a support individual team member who analyzes and executes tasks that are typically routine. Provides inter-departmental support on an ad-hoc basis to support the Production Equipment Repair & Maintenance goals and objectives. Follows and applies routine administrative processes to ensure accuracy, timeliness, and quality of deliverables. Complies with high standards of professionalism, efficiency, personal communication, discretion, and independent judgment. Complies with managerial requirements for core tasks for the support function of the Production Equipment Repair & Maintenance unit, and follows routine administrative processes to ensure accuracy, timeliness, and quality of deliverables. Compiles data to communicate... | |
POSITION SUMMARY The Clinical Lab Scientist Lead is a member of the Operations Department responsible for processing and analyzing specimens and maintaining equipment in good conditions. The individual collaborates with team of CLSs and lab personnel to process samples and perform any troubleshooting as needed. PRIMARY RESPONSIBILITIES Verify the proper specimen being analyzed for patients and perform correct tests that need to be completed Assists the team in day-to-day lab work according to standard operating procedure with little to no errors Follows GLP (good laboratory practice); reports non-conformity of SOPs to supervisor/manager Ensures production work is consistently completed in a... | |
Senior Manager, Oncology Trial NavigationApply →Fresh
Mar 20 $168,100 - $210,100
San Carlos, CASenior Manager, Oncology Trial Navigation About the Role The Senior Manager of Oncology Trial Navigation will play a critical role in connecting Signatera patients to appropriate clinical trial opportunities, sponsored by biopharma partners, academia, or by Natera itself. The Senior Manager will initially serve as the lead individual contributor to establish ground truth for the oncology navigation workflow with the expectation that the role will evolve as the program scales to focus on strategic program growth and team leadership. You will serve as the operational bridge between Natera’s centralized patient screening team and external stakeholders—including treating oncologists, principal... | |
Oncology Trial Navigator About the Role The Oncology Trial Navigator will play a critical role in connecting Signatera patients to life-changing clinical trial opportunities. As a front-line clinical expert, you will be responsible for the end-to-end execution of patient matching workflows—from initial AI-enabled screening to successful enrollment at a clinical trial site. You will serve as the primary clinical point of contact for external stakeholders, including treating oncologists, principal investigators (PIs), and research coordinators. This role combines deep oncology clinical knowledge with high-touch stakeholder engagement in a fast-scaling, mission-driven environment. You will work closely with the Senior Manager of Oncology... | |
The Supervisor of the clinical laboratory is a member of the Operations Department whose role is to oversee employees' performance and serve as a liaison between employees and senior management to meet company goals and quality objectives. The supervisor is responsible for daily supervision of lab staff performing duties such as laboratory testing and data review. Duties include but are not limited to coaching, motivating, staffing, evaluating, and training staff. The supervisor works closely with the manager to ensure company and team goals are met while adhering to good manufacturing practices and CLIA/CAP guidelines. The shift timings are from 3.00... | |
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. The Laboratory for Experimental Medicine (LEM) group oversees internally supported and... | |
Project Coordinator IIIFresh
Mar 20 $54,400 - $81,600 Mounds View, Minnesota, United States of America Apply →Project Coordinator IIIApply →Fresh
Mar 20 $54,400 - $81,600
Mounds View, Minnesota, United States of AmericaAt Medtronic you can begin a life-long career of exploration and innovation, while helping champion access to life-saving therapies for small and underserved patient populations. You will lead with purpose, breaking down barriers to therapy access in a more connected, compassionate world. You will be a member of the Cardiac Rhythm Management (CRM) Released Product Engineering (RPE) team that supports the design and distribution of innovative implantable devices to treat cardiac rhythm disorders. The Project Coordinator III position for Medtronic CRM RPE will be responsible for leading request fulfillment activities for the Special Request Custom/Compassionate Programs. These global programs develop... | |
Executive Director, Global Clinical Trial Operations, OncologyFresh
Mar 20 $255,800 - $402,700 USA - New Jersey - Rahway Apply →Executive Director, Global Clinical Trial Operations, OncologyApply →Fresh
Mar 20 $255,800 - $402,700
USA - New Jersey - RahwayThe Executive Director (ED) is the Clinical Operations lead in a country/ cluster and is responsible for execution of all Clinical Trials in scope for Global Clinical Trial Operations (GCTO) country operations. Adherence to GCP, local and global policies and procedures to conduct high-quality, inspection ready studies is essential. The position is accountable for trial quality and audit responses and completion of CAPAs. The incumbent ensures a single point of contact for managing clinical trial execution in all its aspects across phases in scope of GCTO within the country/cluster. The position has multiple touch points across the company which will... | |
POSITION SUMMARY The Clinical Laboratory Scientist analyzes specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES Verify the proper specimen being analyzed and perform tests that need to be completed Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors Responsible for maintaining updated understanding and knowledge of methods performed in the lab Follows GLP (good laboratory practice) maintain clean and organized work space Completes training and other deadlines on time. Go-to person when lead/supervisor is not available Train on specialized instructions... | |
POSITION SUMMARY Analyzes specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES Verify the proper specimen being analyzed and perform tests that need to be completed Analyze clinical laboratory specimens following the standard methods and procedures in an efficient manner with little to no errors Responsible for maintaining updated understanding and knowledge of methods performed in the lab Follows GLP (good laboratory practice) maintain clean and organized work space Completes training and other deadlines on time. Go-to person when lead/supervisor is not available Assists lead/supervisor in training new hires and/or assists... | |
The Patient Coordinator plays a critical inside sales role in driving the success of Natera’s Oncology product lines. This position is responsible for managing and growing patient relationships while directly contributing to revenue through proactive outreach, pipeline development, and ongoing engagement. As a primary point of contact for patients, the Patient Coordinator partners closely with Field Sales, Operations, and internal stakeholders to execute territory strategies, advance opportunities through the sales pipeline, and ensure timely testing and repeat utilization. This role blends customer advocacy with inside sales execution, requiring strong relationship-building skills, sales acumen, and the ability to connect daily activities... | |
Senior Data Engineer - Clinical Trial DataFresh
Mar 19 $106,500 - $202,500 North Chicago, IL, United States Apply →Senior Data Engineer - Clinical Trial DataApply →Fresh
Mar 19 $106,500 - $202,500
North Chicago, IL, United StatesThe Data Science and Analytics is an ambitious team of Data Scientists and Data Engineers with a unique blend of Business, Scientific, and Machine Learning expertise that seeks to unleash the full potential of AbbVie’s data assets by bringing technology and/or data and insights to the forefront of decision making via fit-for-purpose solutions. The Senior Data Engineer is a key technical leadership role to enable application of advanced analytics techniques across clinical development continuum. Enables Data flow, Data Wrangling, and Data Modeling in support of the advanced analytics techniques like Machine Learning and Visual Analytics. Drives standards and best practices... | |
Pathology Support Coordinator - Sample Review - ASCP Required 2nd Shift T-SFresh
Mar 19 Salary N/A San Carlos, CA Apply →Pathology Support Coordinator - Sample Review - ASCP Required 2nd Shift T-SApply →Fresh
Mar 19 Salary N/A
San Carlos, CAPRIMARY RESPONSIBILITIES Leverage multiple information sources, including LIMS, to review cases for accuracy and completeness of pathology tissue samples for Signatera and Altera testing. Interpret pathology reports, clinical notes and additional testing reports to complete light data entry for each tissue sample. Collaborate with team members to work to resolve potential discrepancies. Ensure that necessary notes and holds are placed on cases for non-conforming samples, discrepancies and/or missing information and escalated to ensure timely resolution. Confirm cancer types for the reporting team before the report is issued via emails and spreadsheet. Meet daily case... | |
POSITION SUMMARY The role of Patient Coordinator will be central to the success of the Renasight product line. This position will be focused on growing the relationship between Natera and its patients to ensure timely management of testing. Core responsibilities include collaborating with Nurse Coordinators to increase revenue and drive market development through direct sales by being the key contact for patient needs. The Patient Coordinator will accomplish this by being the patient advocate within Natera. PRIMARY RESPONSIBILITIES Work with customer care team to maintain & support existing customers. Assess the needs of patients with a focus on customer support,... | |
Senior Clinical Trial Associate (Contractor)Fresh
Remote
Mar 19 Salary N/A United States Apply →Senior Clinical Trial Associate (Contractor)Apply →Fresh
Remote
Mar 19 Salary N/A
United StatesLegend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop... | |
Senior Project CoordinatorFresh
Mar 19 $78,000 - $156,000 United States - Illinois - Abbott Park Apply →Senior Project CoordinatorApply →Fresh
Mar 19 $78,000 - $156,000
United States - Illinois - Abbott ParkWe have an immediate opportunity for a Senior Project Coordinator in our Abbott Park, IL location. The Senior Project Coordinator will support priority initiatives and other HR projects. The ideal candidate will operate with a high degree of collaboration and independence, working closely with Project Manager(s) to drive execution and ensure alignment across cross‑functional teams. Strong organizational and communication skills are essential, as this role frequently collaborates with stakeholders within HR and across other Abbott functions. What You'll Work On Assist in preparing project plans, timelines, and schedules. Organize and facilitate project meetings, including scheduling, drafting agendas, capturing minutes, and... | |
Associate Director - Clinical Research Lead-OncologyFresh
Remote
Mar 19 $115,500 - $204,600 US, Remote Apply →Associate Director - Clinical Research Lead-OncologyApply →Fresh
Remote
Mar 19 $115,500 - $204,600
US, RemoteAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Purpose The Clinical Research Lead (CRL) is a strategic, field-based scientific... | |
Clinical Research AssociateFresh
Mar 19 $73,900 - $116,000 United States - California - Alameda Apply →Clinical Research AssociateApply →Fresh
Mar 19 $73,900 - $116,000
United States - California - AlamedaClinical Research Associate (CRA) Under supervision, the CRA will ensure quality, accuracy, and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155. This is an on-site position in Alameda, California. This is not a remote position. What You'll Work On Under supervision, the incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as assigned by management. Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of action items. Assist and conduct clinical... | |
Associate Clinical Experience Analyst - Genetic Counselor AssistantFresh
Mar 18 $48,000 - $85,000 US - WI - Marshfield Apply →Associate Clinical Experience Analyst - Genetic Counselor AssistantApply →Fresh
Mar 18 $48,000 - $85,000
US - WI - MarshfieldHelp us change lives At Exact Sciences, we’re helping change how the world prevents, detects and guides treatment for cancer. We give patients and clinicians the clarity needed to make confident decisions when they matter most. Join our team to find a purpose-driven career, an inclusive culture, and robust benefits to support your life while you’re working to help others. Position Overview This role delivers clinical expertise and operational support, ensuring accurate handling of medical inquiries and process escalations. It combines training development, cross-functional collaboration, and data-driven analysis to improve workflows and enhance customer experience. This role is in... | |
Senior Toxicologist - Study MonitorFresh
Mar 18 $65,250 - $169,400 US, Indianapolis IN Apply →Senior Toxicologist - Study MonitorApply →Fresh
Mar 18 $65,250 - $169,400
US, Indianapolis INAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our... | |
Clinical Research Physician, GPS MedicalFresh
Mar 18 $198,000 - $356,400 US, Indianapolis IN Apply →Clinical Research Physician, GPS MedicalApply →Fresh
Mar 18 $198,000 - $356,400
US, Indianapolis INAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. The Clinical Research Physician (CRP) in GPS Medical has responsibilities associated... | |
Specialist Projects CoordinatorFresh
Mar 18 $61,300 - $122,700 United States - Ohio - Columbus Apply →Specialist Projects CoordinatorApply →Fresh
Mar 18 $61,300 - $122,700
United States - Ohio - ColumbusWorking at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to Career development with an international company where you can grow the career you dream of. Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with a high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to... | |
Trainer Coordinator Divisional Information In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. This position works out of our Plymouth, MN, location in the Electrophysiology (EP) division. Main Purpose of Role Responsible for the coordination, implementation, and execution of training systems, including developing and innovating training programs to support manufacturing and peripheral groups. Coordinates the ongoing and recurring system training of manufacturing training assistants. Implements and maintains training system controls for manufacturing. What You’ll Work On Develops... | |
Senior Clinical Research ScientistFresh
Mar 18 $78,000 - $156,000 United States - Minnesota - Plymouth Apply →Senior Clinical Research ScientistApply →Fresh
Mar 18 $78,000 - $156,000
United States - Minnesota - PlymouthSenior Clinical Research Scientist This position works out of our St. Paul, MN or Plymouth, MN location in the Electrophysiology division. In Abbott’s Electrophysiology (EP) business, we’re advancing the treatment of heart disease through breakthrough medical technologies in atrial fibrillation, allowing people to restore their health and get on with their lives. As the Senior Clinical Research Scientist you will lead scientific activities associated with the design, conduct, and reporting of clinical trials for this therapeutic area. This position will participate in the development of clinical evidence to establish feasibility, achieve regulatory approvals, meet ongoing regulatory requirements, gain reimbursement,... | |
Clinical Research SpecialistFresh
Mar 18 $83,200 - $124,800 Fridley, Minnesota, United States of America Apply →Clinical Research SpecialistApply →Fresh
Mar 18 $83,200 - $124,800
Fridley, Minnesota, United States of AmericaAs a Clinical Research Specialist, you will leverage relationships with key customers to collect high quality surveillance and outcome data from patients using our products from diverse therapy lines. As a dedicated liaison, you will be responsible for enhancing communications between Medtronic and our customers. This role will interact with multiple stakeholders to accelerate center activation cycle times, proactively manage center performance, and foster strong customer partnerships. In this role, you will work under general supervision to facilitate strong contributions to a registry of market-approved devices. You will exchange informative facts, status updates, ideas and issues to achieve objectives, and... | |
The Project Coordinator’s primary function is to develop, execute, and manage assigned projects and programs in a compliant manner and within budget. The Project Coordinator will drive multiple projects while working directly with key stakeholders and leaders. This role is accountable for managing/coordinating projects that have compliance and budgetary impact to the business. This role has impact by improvement and optimization programs with stakeholders Responsibilities Drive continuous improvements and participate in continuous improvement initiatives led by colleagues Identify innovative ideas and solutions to maximize business opportunities to address challenges in assigned areas of responsibility Maintains and communicates project meeting minutes... | |
Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging advanced capabilities to drive industry leading performance. Partners with study teams, AbbVie internal R&D stakeholders, investigators, and site staff for meaningful and effective engagements positioning AbbVie as the partner of choice in clinical trials. Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience. Responsibilities Considered as the Primary Sponsor Point of contact for the investigative site. Advanced level of competency or experience in providing contextual... | |
Our Team Join the People Services team in Mexico, where we serve as the vital bridge between the organization and our employees across industrial sites. Our purpose is to ensure an exceptional employee experience from day one through continuous development, making sure every person has the tools, information, and support needed to contribute to our mission of chasing the miracles of science. What makes us unique is our comprehensive approach we combine operational excellence with a human touch, working directly with manufacturing teams, unionized personnel, and office employees to create solutions that truly impact their daily work experience. Main responsibilities... | |
Senior Clinical Research Director, OphthalmologyMar 17 $236,250 - $393,750 Washington, DC Apply →Senior Clinical Research Director, OphthalmologyApply →Mar 17 $236,250 - $393,750
Washington, DCJoin the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. The Senior Clinical Research Director (CRD) is an expert clinical lead for one or several indications in the Development of an R&D program and is responsible for leading clinical team(s) to deliver successful clinical trials for novel therapeutics for Ophthalmologic Diseases. The role requires clinical leadership, organization skills, strategically and operationally focused, resourceful individual with capacity to arbitrate to create synergies within the team and with external stakeholders, very good emotional intelligence,... | |
Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. Position Overview Sanofi's Biomarkers & Precision Medicine group, within the Translational Medicine Unit, seeks a senior-level ad Biomarker and Precision Medicine Lead who can shape organizational strategy and drive innovation in biomarker development and precision medicine approaches. This data-driven position focuses on leading the development and implementation of decision enabling translational medicine strategies for our robust pipeline in Immunology, Neurology, Ophthalmology, and Rare Diseases. The role is critical in identifying and validating... | |
Principal CoreValve Therapy Development Specialist - DenverMar 17 $140,000 - $150,000 Denver, Colorado, United States of America Apply →Principal CoreValve Therapy Development Specialist - DenverApply →Mar 17 $140,000 - $150,000
Denver, Colorado, United States of AmericaWe are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. The CoreValve Principal Therapy Development Specialist (TDS) provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-Based Therapies (CBT) and CVG... | |
Senior Clinical Trial Physician, RheumatologyMar 17 $308,700 - $374,075; $275,630 - $333,998 Princeton - NJ - US Apply →Senior Clinical Trial Physician, RheumatologyApply →Mar 17 $308,700 - $374,075; $275,630 - $333,998
Princeton - NJ - USClinical Trial Physician, Rheumatology, Cell Therapy The Clinical Trial Physician, Rheumatology, is the primary source of medical accountability and oversight for one or more clinical trials within the Global Drug Development organization. This position will provide the candidate an opportunity to significantly change the treatment of autoimmune diseases such as lupus, scleroderma, inflammatory myositis and/or rheumatoid arthritis with CAR-T cell therapy. The incumbent will be accountable, alongside the Clinical Development Program Lead, for the development of differentiated and strategic CDPs from phase 2-3 and potentially through to registrational execution. They will be foundational in working with teams in Research, Early... | |
Manager, Clinical Research (Irvine, CA) - Johnson and Johnson MedTech, ElectrophysiologyMar 17 $117,000 - $201,250 Irvine, California, United States of America Apply →Manager, Clinical Research (Irvine, CA) - Johnson and Johnson MedTech, ElectrophysiologyApply →Mar 17 $117,000 - $201,250
Irvine, California, United States of AmericaJohnson & Johnson MedTech Electrophysiology is recruiting for a Clinical Research, Manager, to support the Electrophysiology (EP) business unit based in Irvine, CA. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and profoundly impact health for humanity. Learn more at Fueled... | |
Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and... | |
Environmental Monitoring Program Coordinator (2nd Shift) - Sturgis, MI PlantMar 17 $21 - $42 United States - Michigan - Sturgis Apply →Environmental Monitoring Program Coordinator (2nd Shift) - Sturgis, MI PlantApply →Mar 17 $21 - $42
United States - Michigan - SturgisThis position works out of our Sturgis, MI location in the Abbott Nutrition division. Our Nutrition business develops science-based nutrition products for people of all ages, from helping babies and children grow to keeping adult bodies strong and active. Millions of people around the world count on our leading brands – including Similac®, PediaSure®, Pedialyte®, Ensure®, and Glucerna® – to help them get the nutrients they need to live their healthiest lives. For over 70 years, Abbott’s Sturgis, Mich. , has been impacting its community while producing products that provide essential nutrition to millions of families around the world. Working... | |
Director, Precision Medicine and Diagnostics QualityRemote
Mar 17 $198,507 - $229,864 United States - Remote Apply →Director, Precision Medicine and Diagnostics QualityApply →Remote
Mar 17 $198,507 - $229,864
United States - RemoteDirector, Precision Medicine and Diagnostics Quality In this vital role you will report to the Executive Director, Precision Medicine/Dx and R&D Supplier Quality. The Director, Precision Medicine/Dx provides leadership to a professional quality team who support IVDR, ICH E6 (R3), GCP, and other relevant regulatory requirements and standards related to In-Vitro Diagnostics (IVD), including Digital Diagnostics, Companion Diagnostics (CDx), and Precision Medicine applications in clinical development. This role is responsible for the development and implementation of an end to end, proactive and risk-based Quality Assurance strategy for Precision Medicine and Diagnostics, including third-party collaborations. The Precision Medicine/Dx Quality strategy... | |
Associate Director, Central Monitor - HybridMar 17 $137,500 - $261,000 North Chicago, IL, United States Apply →Associate Director, Central Monitor - HybridApply →Mar 17 $137,500 - $261,000
North Chicago, IL, United StatesThe Central Monitoring Associate Director is responsible for bringing science to life by leading a cross-functional team of Central Monitoring Managers charged with de-risking assigned clinical studies and thereby advancing AbbVie clinical research and development programs. The Central Monitoring Associate Director is accountable for service delivery results (quality, efficient, on-time and on-objective delivery) and for the building and strengthening the talent pipeline for today’s needs and for the leaders of tomorrow. The Associate Director of Central Monitoring role is a manager of manager position that will be filled when organizational size requires this level to manage span of control. Responsibilities... | |
Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging advanced capabilities to drive industry leading performance. Partners with study teams, AbbVie internal R&D stakeholders, investigators, and site staff for meaningful and effective engagements positioning AbbVie as the partner of choice in clinical trials. Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience. Responsibilities Considered as the Primary Sponsor Point of contact for the investigative site. Advanced level of competency or experience in providing contextual... | |
At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Organization Overview At Lilly, we unite caring with discovery to make... | |
Corevalve Senior Therapy Development Specialist - Seattle, WAMar 16 $128,000 - $140,000 Seattle, Washington, United States of America Apply →Corevalve Senior Therapy Development Specialist - Seattle, WAApply →Mar 16 $128,000 - $140,000
Seattle, Washington, United States of AmericaWe are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. The CoreValve Therapy Development Specialist provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-based Therapies (CBT) and CVG field organizations... | |
Senior CoreValve Therapy Development Specialist (Bay Area)Mar 16 $128,000 - $140,000 Bay Area, California, United States of America Apply →Senior CoreValve Therapy Development Specialist (Bay Area)Apply →Mar 16 $128,000 - $140,000
Bay Area, California, United States of AmericaWe are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. The CoreValve Therapy Development Specialist provides technical, clinical, educational and sales support to ensure safe adoption and growth of the Medtronic CoreValve System and future catheter-based therapy technologies. The CoreValve Therapy Development Specialist works closely with implanting teams and the Medtronic Catheter-based Therapies (CBT) and CVG field organizations... | |
Director Clinical Research, SpineMar 16 $164,000 - $282,900 Raynham, Massachusetts, United States of America Apply →Director Clinical Research, SpineApply →Mar 16 $164,000 - $282,900
Raynham, Massachusetts, United States of AmericaAbout Orthopaedics Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Orthopaedics? Ready to join a team that’s reimagining how we heal? Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports, extremities, and elective foot and ankle; spine; and robotics and digital surgery. Your unique talents will help patients on their... | |
Clinical Trial Coordinator IIRemote
Mar 16 $92,000 - $148,350 Danvers, Massachusetts, United States of America Apply →Clinical Trial Coordinator IIApply →Remote
Mar 16 $92,000 - $148,350
Danvers, Massachusetts, United States of AmericaWe are searching for the best talent for Clinical Trial Coordinator II Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients. Your unique talents will help patients on their journey to wellness. Learn... | |
Sr Mgr Global Trial OptimizationRemote
Mar 16 $134,400 - $219,200 Remote - United States Apply →Sr Mgr Global Trial OptimizationApply →Remote
Mar 16 $134,400 - $219,200
Remote - United StatesThe Senior Manager, Global Trial Optimization will lead program or study level activities advising on our clinical development strategy, clinical study concepts, study protocols and operational plans that will enable predictable delivery of clinical programs and studies. You will develop and maintain relationships with our external experts facilitating a wide source of country and disease area intelligence used in study design and operational planning. A typical day may include the following Lead study level feasibility processes to generate high quality and timely data to inform study design, efficient geographical placement and operational planning. Partner with teams during CRO... | |
Senior Manager, Global Trial OptimizationRemote
Mar 16 $134,400 - $219,200 Remote - United States Apply →Senior Manager, Global Trial OptimizationApply →Remote
Mar 16 $134,400 - $219,200
Remote - United StatesThe Senior Manager, Global Trial Optimization will lead program or study level activities advising on our clinical development strategy, clinical study concepts, study protocols and operational plans that will enable predictable delivery of clinical programs and studies. You will develop and maintain relationships with our external experts facilitating a wide source of country and disease area intelligence used in study design and operational planning. A typical day may include the following Lead study level feasibility processes to generate high quality and timely data to inform study design, efficient geographical placement and operational planning. Partner with teams during... | |
Clinical Research Associate Type Remote - Field - Chicago/Wisconsin The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Manager to ensure that study commitments are achieved in a timely and efficient manner. The CRA acts as the main contact with the study site and has the responsibility for monitoring the study conduct to ensure proper delivery of the study. The CRA is responsible for the preparation,... | |
Principal Scientist, Clinical Research, ImmunologyMar 16 $250,800 - $394,800 USA - New Jersey - Rahway Apply →Principal Scientist, Clinical Research, ImmunologyApply →Mar 16 $250,800 - $394,800
USA - New Jersey - RahwayThe Clinical Director (Principal Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a focus on late-stage development, the Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Clinical Director May Be Responsible For Evaluating pre-clinical and translational work for the purpose of generating the early clinical development plan and Investigational New Drug applications. Providing clinical development support of business development assessments of external opportunities to grow... | |
Clinical Research, Associate IMar 16 $73,900 - $116,000 United States - California - Alameda Apply →Clinical Research, Associate IApply →Mar 16 $73,900 - $116,000
United States - California - AlamedaClinical Research Associate I The CRA will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155. This is an on-site position in Alameda, California. What You’ll Work On Perform internal clinical studies, recruit study participants, conduct informed consent discussions with study volunteers, record study data, and maintain study files. Coordinate internal clinical studies from start to close-out. Perform study site visits (SQV, SIV, IMV, COV), generate monitoring reports, and track resolution of action items. Assist and conduct clinical monitoring and... | |
Clinical Trial Physician, NeuroscienceMar 16 $273,210 - $331,063; $243,930 - $295,589 Cambridge Crossing - MA - US Apply →Clinical Trial Physician, NeuroscienceApply →Mar 16 $273,210 - $331,063; $243,930 - $295,589
Cambridge Crossing - MA - USThe Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a high performing Study Delivery Team... | |
Clinical Associate Our Abbott story is one of delivering bold solutions in the face of complex healthcare challenges. At Abbott Electrophysiology (EP), we’ve been a leader for over 20 years, pioneering one of the first mapping systems, introducing the first contact force ablation catheter and creating a portfolio of products trusted in millions of procedures around the world. We have and will continue to redefine what’s possible in an evolving and challenging EP landscape. When you join Abbott EP, you become part of a passionate group of individuals who are dedicated to driving the EP space forward and... | |
Advance AbbVie's pipeline by striving for excellence in clinical research, turning science into medicine for our patients and leveraging new advanced capabilities to drive industry leading performance. Partners with the investigator and site staff for meaningful and effective engagements positioning AbbVie as the choice in clinical trials. Focus on site clinical research that ensures appropriate conduct of the trial while driving improvement in data integrity, compliance, overall study performance and customer experience. Responsibilities Considered as the primary point of contact for the investigative site. High level of competency or experience in providing contextual information on the clinical trials, connects stakeholder... | |
POSITION SUMMARY Responsible for daily supervision of lab staff performing duties such as laboratory testing and data review. Duties include but are not limited to coaching, motivating, staffing, evaluating, and training staff. Works closely with Manager to ensure company, department, and team goals are met. PRIMARY RESPONSIBILITIES Responsible for day-to-day staffing/scheduling/setting up sample run schedules. Ensures production work is consistently completed according to department goals. Ensures all case samples are processed and accounted for. Monitors team members to ensure adherence to SOPs and safety procedures Oversees training for new hires works in conjunction with lead to train new hires.... | |
Under moderate supervision, coordinates and consolidates finished goods inventory from manufacturing to support order fulfillment. Primary responsibilities are to provide support in Logistics and Materials for all product lines and to coordinate shipments to customers through inventory control. These job duties will be performed in compliance with established global standard procedures. Helps segregate short dated and expired material, scrap requests, perform cycle counts, transport material to and from offsite storage, reconcile inventory discrepancies, and proper location transfers for finished goods inventory. Ensures documentation is followed according to procedure. Support picking, packing and processing for order fulfillment. Responsibilities Transfer finished goods... | |
Travel Experience CoordinatorMar 13 $61,300 - $122,700 United States > Austin : 8701 Bee Caves Rd Apply →Travel Experience CoordinatorApply →Mar 13 $61,300 - $122,700
United States > Austin : 8701 Bee Caves RdAt Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You’ll also have access to Career development with an international company where you can grow the career you dream of . Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year. An excellent retirement savings plan with high employer contribution Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.... | |
Sr Administrative CoordinatorMar 13 $126,820 - $164,120 United States - California - Foster City Apply →Sr Administrative CoordinatorApply →Mar 13 $126,820 - $164,120
United States - California - Foster CityGilead's mission is to discover, develop, and deliver therapies that will improve the lives of patients with life-threatening illnesses worldwide. This position performs a wide variety of activities in support of the SVP and their respective organization. Key Responsibilities Handling complex projects and events that require gathering, reviewing, and analyzing data that impact a major portion of the organization. Serves as a primary resource for data and information to others in their function, and represents the function on administrative matters. May recommend, interpret, and/or implement company and internal administrative policies and procedures, and interprets administrative policies and procedures when... | |
Project Coordinator IV, CRM (East Coast)Mar 12 $62,400 - $93,600 Charlotte, North Carolina, United States of America Apply →Project Coordinator IV, CRM (East Coast)Apply →Mar 12 $62,400 - $93,600
Charlotte, North Carolina, United States of AmericaWe are seeking a committed professional to join our team. While this is a remote position not located at a physical Medtronic site, the candidate hired will be required to reside within the territory and drive to multiple accounts throughout the region. A valid driver's license is essential for this role. We are looking for a highly motivated individual interested in cultivating their career focused on advancing the Medtronic Mission. Communicates with internal and external stakeholders including customers and physician partners. Organizes, attends, participates in, and sends follow-up communications for team meetings Provides support in preparing presentation materials and... | |
Payment Specialist - Clinical Trial Financial OperationsRemote
Mar 12 $95,000 - $124,000 Remote, USA Apply →Payment Specialist - Clinical Trial Financial OperationsApply →Remote
Mar 12 $95,000 - $124,000
Remote, USAAbout This Role As a Payment Specialist in Clinical Trial Financial Operations - Pharma/Biotech , you will play a crucial role in the management of investigator payments, ensuring timeliness, accuracy, and compliance with clinical trial agreements. Situated within the Site Contracts Management team, you will lead interactions with study teams, budget hubs, and EDC functional groups to set up and manage payments effectively. Your role will involve drafting and finalizing payment terms, leading monthly reporting meetings with payment vendors, and resolving payment disputes to support our clinical trials. The value of this position lies in its impact on the seamless... | |
What you will do In this vital role you will providing administrative and operational support to the Vice President of Finance. This role requires strong organizational skills, attention to detail, and the ability to manage multiple priorities in a fast-paced, global environment. The Sr EA serves as a key enabler to optimize the executive’s time and effectiveness. The role requires excellent judgment, discretion, and the ability to manage multiple priorities with efficiency and tact. Key Responsibilities Executive Support Maintain confidentiality and manage sensitive information with the utmost discretion. Manage and prioritize complex calendar and meeting schedules across global time... | |
POSITION SUMMARY Natera is currently seeking a Clinical Laboratory Associate to analyze laboratory specimens following the standard methods and procedures while maintaining equipment and instruments in good operating condition by troubleshooting malfunctions as needed. PRIMARY RESPONSIBILITIES Assists in testing of patient samples according to standard operating procedure in an efficient manner with little to no errors Responsible for maintaining updated understanding and knowledge of methods performed in the lab Follows GLP (good laboratory practice) maintain cleans and organized work space Completes training and other deadlines on time. Recognizes and escalates equipment malfunctions; troubleshoots common errors on the lab floor Recognizes,... | |
POSITION SUMMARY The Natera Test Coordinator plays a vital role in ensuring a seamless testing experience for patients. This position is responsible for scheduling and determining the most effective method for blood collection, preparing specimens for laboratory testing, and managing all necessary paperwork to ensure compliance. In this role, you will work closely with customers and the sales team to facilitate an efficient ordering process and timely reporting of results. The ideal candidate thrives in an independent work environment, excels at multitasking, and demonstrates strong critical thinking skills to resolve issues promptly. *This is a clinic based role... | |
POSITION SUMMARY The Natera Test Coordinator plays a vital role in ensuring a seamless testing experience for patients. This position is responsible for scheduling and determining the most effective method for blood collection, preparing specimens for laboratory testing, and managing all necessary paperwork to ensure compliance. In this role, you will work closely with customers and the sales team to facilitate an efficient ordering process and timely reporting of results. The ideal candidate thrives in an independent work environment, excels at multitasking, and demonstrates strong critical thinking skills to resolve issues promptly. *This is a clinic based role... | |
POSITION SUMMARY The Natera Test Coordinator plays a vital role in ensuring a seamless testing experience for patients. This position is responsible for scheduling and determining the most effective method for blood collection, preparing specimens for laboratory testing, and managing all necessary paperwork to ensure compliance. In this role, you will work closely with customers and the sales team to facilitate an efficient ordering process and timely reporting of results. The ideal candidate thrives in an independent work environment, excels at multitasking, and demonstrates strong critical thinking skills to resolve issues promptly. *This is a clinic based role... | |
POSITION SUMMARY The Natera Test Coordinator plays a vital role in ensuring a seamless testing experience for patients. This position is responsible for scheduling and determining the most effective method for blood collection, preparing specimens for laboratory testing, and managing all necessary paperwork to ensure compliance. In this role, you will work closely with customers and the sales team to facilitate an efficient ordering process and timely reporting of results. The ideal candidate thrives in an independent work environment, excels at multitasking, and demonstrates strong critical thinking skills to resolve issues promptly. *This is a clinic based role... | |
Senior Principal Scientist, Clinical Research, NeuroscienceMar 12 $276,600 - $435,400 USA - New Jersey - Rahway Apply →Senior Principal Scientist, Clinical Research, NeuroscienceApply →Mar 12 $276,600 - $435,400
USA - New Jersey - RahwayOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards. The Senior Director (Senior Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Neuroscience Medicines. Our company's Neuroscience Medicines span all phases of clinical development (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical... | |
Associate Director - Statistics (Clinical Trial)Mar 11 $137,500 - $261,000 Irvine, CA, United States Apply →Associate Director - Statistics (Clinical Trial)Apply →Mar 11 $137,500 - $261,000
Irvine, CA, United StatesThe Associate Director, Statistics provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients. Responsibilities Provide statistical support for one or more clinical development projects through own efforts or those of a team. Lead/develop statistical strategy for project development and regulatory submission. Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans. Represent function/department... | |
Associate Director - Statistics (Clinical Trial)Mar 11 $137,500 - $261,000 Florham Park, NJ, United States Apply →Associate Director - Statistics (Clinical Trial)Apply →Mar 11 $137,500 - $261,000
Florham Park, NJ, United StatesThe Associate Director, Statistics provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients. Responsibilities Provide statistical support for one or more clinical development projects through own efforts or those of a team. Lead/develop statistical strategy for project development and regulatory submission. Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans. Represent function/department... | |
Associate Scientific Director, Translational Precision Medicine, NeuroscienceMar 11 $137,500 - $261,000 Waltham, MA, United States Apply →Associate Scientific Director, Translational Precision Medicine, NeuroscienceApply →Mar 11 $137,500 - $261,000
Waltham, MA, United StatesPurpose As a translational scientist in Precision Medicine Neuroscience bridges basic brain and nervous system research and clinical applications, focusing on developing biological and disease insights for neurological and psychiatric disorders. Responsibilities Uncover neurobiological mechanisms of disease that elucidate patient subtypes; mechanisms of action, response, or resistance, and advance the development of novel interventions. Develop testable hypotheses related to neurobiological pathways, neuronal circuitry, cognitive or behavioral domains, or functional markers of disease or patient subtypes that will advance pipeline and disease area goals. Collaborate with PMed DAS leads and other functional leads, develop and execute operationally-sound approach and generate actionable... | |
Scientific Director I, Translational Precision Medicine, NeuroscienceMar 11 $156,000 - $296,500 Waltham, MA, United States Apply →Scientific Director I, Translational Precision Medicine, NeuroscienceApply →Mar 11 $156,000 - $296,500
Waltham, MA, United StatesPurpose As a translational scientist in Precision Medicine Neuroscience bridges basic brain and nervous system research and clinical applications, focusing on developing biological and disease insights for neurological and psychiatric disorders. Responsibilities Uncover neurobiological mechanisms of disease that elucidate patient subtypes; mechanisms of action, response, or resistance, and advance the development of novel interventions. Develop testable hypotheses related to neurobiological pathways, neuronal circuitry, cognitive or behavioral domains, or functional markers of disease or patient subtypes that will advance pipeline and disease area goals. Collaborate with PMed DAS leads and other functional leads, develop and execute / drive execution of operationally-sound... | |
Associate Director - Statistics (Clinical Trial)Mar 11 $137,500 - $261,000 North Chicago, IL, United States Apply →Associate Director - Statistics (Clinical Trial)Apply →Mar 11 $137,500 - $261,000
North Chicago, IL, United StatesThe Associate Director, Statistics provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients. Responsibilities Provide statistical support for one or more clinical development projects through own efforts or those of a team. Lead/develop statistical strategy for project development and regulatory submission. Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans. Represent function/department... | |
Scientific Director II, Translational Precision Medicine, NeuroscienceMar 11 $177,000 - $336,000 Waltham, MA, United States Apply →Scientific Director II, Translational Precision Medicine, NeuroscienceApply →Mar 11 $177,000 - $336,000
Waltham, MA, United StatesPurpose As a translational scientist in Precision Medicine Neuroscience bridges basic brain and nervous system research and clinical applications, focusing on developing biological and disease insights for neurological and psychiatric disorders. Responsibilities Uncover neurobiological mechanisms of disease that elucidate patient subtypes; mechanisms of action, response, or resistance, and advance the development of novel interventions. Develop testable hypotheses related to neurobiological pathways, neuronal circuitry, cognitive or behavioral domains, or functional markers of disease or patient subtypes that will advance pipeline and disease area goals. Collaborate with PMed DAS leads and other functional leads, develop and execute operationally-sound approach and generate actionable... | |
Associate Director - Statistics (Clinical Trial)Mar 11 $137,500 - $261,000 South San Francisco, CA, United States Apply →Associate Director - Statistics (Clinical Trial)Apply →Mar 11 $137,500 - $261,000
South San Francisco, CA, United StatesThe Associate Director, Statistics provides statistical leadership for clinical development and life-cycle management strategies for assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs. The Associate Director works in partnership with experts in multiple disciplines to advance medicines to our patients. Responsibilities Provide statistical support for one or more clinical development projects through own efforts or those of a team. Lead/develop statistical strategy for project development and regulatory submission. Provide statistical leadership for design, analysis and reporting for clinical or other scientific research programs. Independently develop protocols and statistical analysis plans. Represent function/department... | |
US: Senior Clinical Research ScientistMar 11 $142,146 - $186,567 Somerset, New Jersey, United States Apply →US: Senior Clinical Research ScientistApply →Mar 11 $142,146 - $186,567
Somerset, New Jersey, United StatesLegend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide. Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop... | |
Sr. Coordinator, Patient AccessMar 11 $103,300 - $141,000 US CA San Diego Apply →Sr. Coordinator, Patient AccessApply →Mar 11 $103,300 - $141,000
US CA San DiegoSupports broader Patient Access and works with general guidance and assumes responsibility for a definable portion of projects and coordination of all department initiatives, budget tracking, meeting support, and other project activity as assigned. Oversees team Calendar and logistics associated with team and cross-functional meetings. Creates and edits Excel, PowerPoint and other project documentation in support of department initiatives. _ Your Contributions (include, but are not limited to) Creates and manages coordination of communication across Patient Access initiatives Manages Patient Access team calendars, rosters, and shared documents on company intranet website (SharePoint) Oversees and manages all aspects of new hire... | |
Senior Director, Oncology Clinical Trial OperationsMar 11 $265,800 - $332,200 San Carlos, CA Apply →Senior Director, Oncology Clinical Trial OperationsApply →Mar 11 $265,800 - $332,200
San Carlos, CAPOSITION SUMMARY The Senior Director, Oncology Clinical Trials will lead the strategic planning and operational execution of oncology clinical trials evaluating Natera’s oncology products, with primary focus on Natera Sponsored interventional studies. Additional oncology portfolio support may be added over time. This role is responsible for feasibility assessment, enrollment modeling, timeline forecasting, budget development, and end-to-end study execution. The position requires a strong program management leader who can build scalable operational frameworks, manage CRO partnerships, lead cross-functional teams, and ensure high-quality data generation to support clinical utility, regulatory, and commercial objectives. This individual will serve as a key... | |
Sr. Clinical Trial PhysicianMar 11 $243,930 - $295,589 Madison - Giralda - NJ - US Apply →Sr. Clinical Trial PhysicianApply →Mar 11 $243,930 - $295,589
Madison - Giralda - NJ - USFunctional Area Description The Senior Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for multiple clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities Provides medical and scientific expertise to cross-functional BMS colleagues Position Responsibilities Medical Monitoring Contributes to and is a key member of a... | |
Clinical Research Leader, NeurovascularMar 10 $109,000 - $174,800 Irvine, California, United States of America Apply →Clinical Research Leader, NeurovascularApply →Mar 10 $109,000 - $174,800
Irvine, California, United States of AmericaJohnson & Johnson MedTech, Neurovascular, is recruiting a Clinical Research Leader, Neurovascular to join our team. This position is located in Irvine, CA. At management discretion, the position may be performed remotely. At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow and... | |
Clinical Trial Physician, NeuropsychiatryMar 10 $308,700 - $374,075; $275,630 - $333,998 Cambridge Crossing - MA - US Apply →Clinical Trial Physician, NeuropsychiatryApply →Mar 10 $308,700 - $374,075; $275,630 - $333,998
Cambridge Crossing - MA - USClinical Trial Physician EMPLOYEE JOB PROFILE (EJP) – Date Modified 25-February-2020 Job Title Clinical Trial Physician (CTP) Division R&D / Global Drug Development Functional Area Description The Clinical Trial Physician sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug development. Clinical Development drives clinical development strategy, design, execution, and interpretation of clinical trials. / Objective Serves as a primary source of medical accountability and oversight for clinical trials Matrix management responsibilities across the internal and external network Manages Phase 1 – Phase 3 studies, with demonstrated decision making capabilities... | |
Twist Bioscience is looking for a seasoned, team-oriented, Shipping Coordinator. This position will play a critical role in forming a best in class Shipping/Order Fulfillment team. This position will require collaboration with Manufacturing, Customer Support, and Supply Chain teams to ensure internal and external customer satisfaction. The Shipping Coordinator will perform all physical and administrative required for this position. This will include inventory management, continuous improvement, shipping, receiving, storing, distributing of orders, materials, parts, supplies and equipment. Must possess a team and collaborative attitude. Shift Thurs-Mon Responsibilities Order fulfillment Perform inventory audit, reconciliation and inspection of finished goods and raw... | |
Associate Coordinator - Biorepository Center of ExcellenceMar 10 $69,000 - $99,667 Swiftwater, PA Apply →Associate Coordinator - Biorepository Center of ExcellenceApply →Mar 10 $69,000 - $99,667
Swiftwater, PASanofi is recruiting for a Biorepository Center of Excellence (BCOE) Associate Coordinator to ensure the local implementation of the new Biosamples Management (BSM) processes in Waltham site in coordination with Sanofi Pharma. This role is accountable for oversight of all local BSM related topics on site through interaction with relevant local stakeholders and training of Waltham personnel on best practices for handling of Human Biological Samples (HBS). The BCOE Associate Coordinator will coordinate local BCOE inventories in a performant and cost-efficient way, in compliance with global BCOE governance and local regulations and in close collaboration with local functions and external... | |
Associate Director - Clinical Research Lead-Oncology (Minnesota, Illinois, Indiana, Ohio, Michigan, Wisconsin)Remote
Mar 10 $115,500 - $204,600 US, Remote Apply →Associate Director - Clinical Research Lead-Oncology (Minnesota, Illinois, Indiana, Ohio, Michigan, Wisconsin)Apply →Remote
Mar 10 $115,500 - $204,600
US, RemoteAt Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Purpose The Clinical Research Lead (CRL) is a strategic, field-based scientific... | |
At Caris, we understand that cancer is an ugly word—a word no one wants to hear, but one that connects us all. That’s why we’re not just transforming cancer care—we’re changing lives. We introduced precision medicine to the world and built an industry around the idea that every patient deserves answers as unique as their DNA. Backed by cutting-edge molecular science and AI, we ask ourselves every day “What would I do if this patient were my mom?” That question drives everything we do. But our mission doesn’t stop with cancer. We're pushing the frontiers of medicine and leading a... | |
Senior Director, Clinical Research, AtherosclerosisMar 10 $276,600 - $435,400 USA - New Jersey - Rahway Apply →Senior Director, Clinical Research, AtherosclerosisApply →Mar 10 $276,600 - $435,400
USA - New Jersey - RahwayThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and studies, including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director May Be Responsible For Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New... | |
Human Resources Coordinator - Talent Acquisition (Contract)Mar 10 $20 - $41 United States - Illinois - Abbott Park Apply →Human Resources Coordinator - Talent Acquisition (Contract)Apply →Mar 10 $20 - $41
United States - Illinois - Abbott ParkThe Opportunity Join Abbott’s Corporate Human Resources team at our global headquarters in Abbott Park, IL. As a Talent Acquisition Coordinator, you’ll play a key role in supporting U.S. recruiting operations and ensuring a smooth, high‑quality experience for candidates and hiring teams. You’ll work across multiple programs, processes, and stakeholders, making a measurable impact on how we attract top talent. This is a long‑term contract role with significant exposure across HR and Talent Acquisition. What You’ll Work On Manage key steps in the hiring process, including background checks and drug screenings. Coordinate high‑volume phone, onsite, and digital interviews across multiple... | |
Director, Global Trial LeadMar 10 $238,890 - $289,482; $213,300 - $258,468 Princeton - NJ - US Apply →Director, Global Trial LeadApply →Mar 10 $238,890 - $289,482; $213,300 - $258,468
Princeton - NJ - USThe Director, Global Trial Lead (GTL) is accountable for the strategic leadership and operational excellence of global clinical trials, driving delivery across all phases and therapeutic areas. This role sets the vision for successful trial execution, influences organizational strategy, and ensures alignment with business objectives, regulatory standards, and quality benchmarks. As a senior leader within Global Development Operations (GDO), the Director GTL is responsible for critical decision making, risk management, and fostering a culture of innovation and continuous improvement. Works closely with internal and external stakeholders, identifying, defining and executing meaningful and targeted process improvement initiatives, supporting strategic planning efforts.... | |
Purpose Efficiently create and execute consulting, sponsorship and/or promotional speaker contracts commensurate with AbbVie’s policies and objectives, while adhering to a strict standard of business ethics and integrity. This position is responsible for contract creation, negotiation, and implementation of agreements to support client initiatives in order to deliver consulting, promotional speaker services or sponsorship benefits to meet critical business needs and customer expectations. This position is responsible for managing the end-to-end Sponsorship process and end-to-end Speaker program process including nominations, FMV and contract execution. works closely with external consultants, speakers, institutions, and large non-profit organizations and with business stakeholders, Legal,... | |
Administrative CoordinatorApply →Mar 9 $99,705 - $129,030
United States - California - La VerneWe are seeking a motivated Administrative Coordinator to support the Site Head of Manufacturing Operations and the leadership team in La Verne, California. This role provides administrative support across a highly matrixed organization and works closely with other site administrative staff. A key part of the role involves driving employee engagement and supporting small projects . This is an excellent opportunity for someone with experience who is looking to get their foot in the door at a large, patient‑focused organization. Ideal candidate will be proactive, resourceful, customer‑service oriented, and professional. This is a fully onsite role, based at our La... | |
Principal Clinical Research Scientist - Equipment Platform VisionMar 9 $134,000 - $231,150 Milpitas, California, United States of America Apply →Principal Clinical Research Scientist - Equipment Platform VisionApply →Mar 9 $134,000 - $231,150
Milpitas, California, United States of AmericaAbout Vision Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.... | |
Principal Clinical Research Scientist - Surgical Implants VisionMar 9 $117,000 - $201,250; $134,000 - $231,150 Irvine, California, United States of America Apply →Principal Clinical Research Scientist - Surgical Implants VisionApply →Mar 9 $117,000 - $201,250; $134,000 - $231,150
Irvine, California, United States of AmericaAbout Vision Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding on the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime.... | |