Clinical Operations Jobs in Pharma & Biotech
63
Open Positions
6
Remote Jobs
55
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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| Company & Role | |
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Clinical Research ManagerFresh
Feb 6 $117,000 - $201,250 Irvine, California, United States of America Apply →Clinical Research ManagerApply →Fresh
Feb 6 $117,000 - $201,250
Irvine, California, United States of AmericaFueled 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 more at We are searching for the best talent for a Clinical... | |
Manager, Clinical Research (Irvine, CA) Johnson and Johnson MedTech, ElectrophysiologyFresh
Feb 6 $117,000 - $201,250 Irvine, California, United States of America Apply →Manager, Clinical Research (Irvine, CA) Johnson and Johnson MedTech, ElectrophysiologyApply →Fresh
Feb 6 $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... | |
Manager, Clinical Research (Irvine, CA) - Johnson and Johnson MedTech, ElectrophysiologyFresh
Feb 6 $117,000 - $201,250 Irvine, California, United States of America Apply →Manager, Clinical Research (Irvine, CA) - Johnson and Johnson MedTech, ElectrophysiologyApply →Fresh
Feb 6 $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... | |
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. Purpose The purpose of the Clinical Trial Quality Associate – Global... | |
Logistics Coordinator - Sturgis, MI PlantFresh
Feb 6 $21 - $42 United States - Michigan - Sturgis Apply →Logistics Coordinator - Sturgis, MI PlantApply →Fresh
Feb 6 $21 - $42
United States - Michigan - SturgisJob Title Logistics Coordinator Shift This position will work 700am to 330pm Monday through Friday and occasional weekends as needed. This 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.... | |
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.... | |
Sr Manager, Case Mgmt, Clinical Trial SafetyFresh
Feb 5 $141,000 - $188,000 Cambridge, MA Apply →Sr Manager, Case Mgmt, Clinical Trial SafetyApply →Fresh
Feb 5 $141,000 - $188,000
Cambridge, MAAbout This Role The Sr Manager Case Management, Clinical Trial Safety will be responsible for managing the in-house case processing of clinical trial safety reports (and some post-market reports) in Biogen’s safety database. This role includes hands-on case processing and QC of ICSRs, workflow management, quality management, responsibility for the SMP and team line management. The Sr Manager will ensure consistent, on time and high-quality output of clinical trial ICSRs, working with cross-functional stakeholders. The Sr Manager will report to the Director of Clinical Trial Safety Operations within the Global Case Management function of Safety & Regulatory Operations, Medical Writing... | |
POSITION SUMMARY ** This position is not remote, it is located on site in San Antonio, TX** 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... | |
Warehouse CoordinatorFresh
Feb 5 $18 - $37 United States > Itasca - AMDC : 1015 West Devon Ave Apply →Warehouse CoordinatorApply →Fresh
Feb 5 $18 - $37
United States > Itasca - AMDC : 1015 West Devon AveThe Opportunity The Warehouse Coordinator is responsible for all distribution activities associated with the shipment of Diagnostic Division reagents and accessories to customers, affiliates and research facilities. Some of these items do not have a assigned commodity number in the inventory management system known as AMM or in the Distribution Floor Control system. For this reason these items must be shipped outside the Distribution Floor Control system using a manual process. The dock warehouse coordinator oversees this process and ensures materials are properly shipped as per all transportation regulations. In addition, the Warehouse Coordinator processes inventory and prepares for ocean... | |
Warehouse CoordinatorFresh
Feb 5 $18 - $37 United States > Itasca - AMDC : 1015 West Devon Ave Apply →Warehouse CoordinatorApply →Fresh
Feb 5 $18 - $37
United States > Itasca - AMDC : 1015 West Devon AveThe Opportunity The Warehouse Coordinator is responsible for all distribution activities associated with the shipment of Diagnostic Division reagents and accessories to customers, affiliates and research facilities. Some of these items do not have a assigned commodity number in the inventory management system known as AMM or in the Distribution Floor Control system. For this reason these items must be shipped outside the Distribution Floor Control system using a manual process. The dock warehouse coordinator oversees this process and ensures materials are properly shipped as per all transportation regulations. In addition, the Warehouse Coordinator processes inventory and prepares for ocean... | |
Clinical Trial Project Manager, Clinical Delivery-EMPFresh
Feb 5 $65,250 - $165,000 US, Indianapolis IN Apply →Clinical Trial Project Manager, Clinical Delivery-EMPApply →Fresh
Feb 5 $65,250 - $165,000
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. Purpose The purpose of the Clinical Trial Project Manager (CTPM) role... | |
Principal Clinical Research Scientist - Surgical Implants VisionFresh
Feb 5 $117,000 - $201,250; $134,000 - $231,150 Irvine, California, United States of America Apply →Principal Clinical Research Scientist - Surgical Implants VisionApply →Fresh
Feb 5 $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.... | |
Principal Clinical Research Scientist - Equipment Platform VisionFresh
Feb 5 $134,000 - $231,150 Milpitas, California, United States of America Apply →Principal Clinical Research Scientist - Equipment Platform VisionApply →Fresh
Feb 5 $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.... | |
Customer Service Support CoordinatorFresh
Feb 4 $79,400 - $128,500 United States - Tennessee - Memphis Apply →Customer Service Support CoordinatorApply →Fresh
Feb 4 $79,400 - $128,500
United States - Tennessee - MemphisROLE SUMMARY The Customer Service Support Coordinator is responsible for providing support services for the Memphis Customer Service team to advance small to mid-size projects, improve operational efficiency, and ensure high quality customer service. The position does not have direct reports, but strong team-based leadership skills are required. This position supports the strategy of the department and will work closely with the Manager, Customer Service, providing back up to this position as needed. The position requires technical acumen, analytical skills, strong project management capabilities, and a good understanding of order to cash processes and activities. This individual will work cross... | |
Senior Manager Global Partnerships & Trial OptimizationFresh
Remote
Feb 4 $134,400 - $219,200 Remote - United States Apply →Senior Manager Global Partnerships & Trial OptimizationApply →Fresh
Remote
Feb 4 $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... | |
Hims & Hers is the leading health and wellness platform, on a mission to help the world feel great through the power of better health. We are redefining healthcare by putting the customer first and delivering access to care that is affordable, accessible, and personal, from diagnosis to treatment to delivery. No two people are the same, so we provide access to personalized care designed for results. By normalizing health & wellness challenges and innovating on their solutions, we’re making better health outcomes easier to achieve. Hims & Hers is a public company, traded on the NYSE under the ticker... | |
Biogen’s West Coast Hub, based in South San Francisco, is specifically focused on transforming the lives of patients with severe immune-mediated diseases by developing novel targeted therapies with outsized clinical impact, faster. To accomplish this, we are seeking top talent to join us on our journey. In alignment with established procedures and SOPs, the Senior Manager, CTL, leverages their phase, indication and operational expertise to independently oversee one or more clinical studies, including Partnering with cross-functional representatives to drive the development of operationally feasible and robust protocol designs, ensuring that principles of patient focus, risk management, quality and scientific integrity... | |
Help 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 The Sr. Clinical Trial Manager (CTM) is responsible for supporting or leading the management, planning, execution, and closure of clinical studies. The Sr. CTM works collaboratively and cross-functionally in an exciting, fast paced environment to oversee the day-to-day... | |
Contract - Facilities CoordinatorApply →Fresh
Feb 4 Salary N/A
Phoenix, AZ - 85040At 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... | |
At Gilead our pursuit of a healthier world for all people has yielded a cure for hepatitis C, revolutionary improvements in HIV treatment and prevention as well as advancements in therapies for viral and inflammatory diseases and certain cancers. We set and achieve bold ambitions in our fight against the world’s most devastating diseases, united in our commitment to confronting the largest public health challenges of our day and improving the lives of patients for generations to come. The Administrative Coordinator to the Senior Vice President (SVP), Treasurer & Head of Investor Relations will partner with our SVP to ensure... | |
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... | |
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 helping people live longer,... | |
Clinical Trial Budget and Contracts ManagerFresh
Remote
Feb 3 $114,700 - $143,400 US Remote Apply →Clinical Trial Budget and Contracts ManagerApply →Fresh
Remote
Feb 3 $114,700 - $143,400
US RemotePOSITION SUMMARY Job Function Clinical Operations Budgets & Contracts Manager As a member of the Clinical Operations team, the Budgets & Contracts Manager i s responsible for managing clinical agreements, budgets, payment follow-up, and corresponding processes in support of the department. This individual should have experience in managing all aspects of study contracts and payments and is expected to provide functional expertise to ensure that timelines, costs, and quality metrics are met and that the study contract is managed in compliance with the study protocol. The Budgets & Contracts Manager works closely with study teams, clinical site personnel, and... | |
POSITION SUMMARY 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... | |
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. Verve Therapeutics, a wholly owned subsidiary of Eli Lilly & Company... | |
Project Coordinator V - Office of the CEOFresh
Feb 3 $75,200 - $112,800 Fridley, Minnesota, United States of America Apply →Project Coordinator V - Office of the CEOApply →Fresh
Feb 3 $75,200 - $112,800
Fridley, Minnesota, United States of AmericaBring your talents to an industry leader in medical technology and healthcare solutions – we’re a market leader and growing every day. You can be proud to be a part of technologies that are rooted in our long history of mission-driven innovation. You will be empowered to shape your own career. We support your growth with the training, mentorship, and guidance you need to own your future success. Together, we can transform healthcare. The Project Coordinator V is a key member of the Portfolio Management and Office of the CEO (OCEO) team, reporting directly to the SVP of Portfolio Management.... | |
Sr Administrative CoordinatorFresh
Feb 3 $126,820 - $164,120 United States - California - Foster City Apply →Sr Administrative CoordinatorApply →Fresh
Feb 3 $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. The Senior Administrative Coordinator will support the SVP of FP&A and VP, Commercial Finance as well as the FP&A Leadership Team, with primary support for an SVP lead (~300 total employees). Key Responsibilities Understand the goals and objectives of FP&A to contribute to its attainment and to help implement them into the culture of the department. Resource to other administrative assistants and is cross trained to provide backfill support. Strategically analyze business operational processes by gathering data to implement solutions;... | |
Principal Risk Based Quality Management Data MonitorFresh
Feb 3 $116,000 - $155,000 Research Triangle Park, NC Apply →Principal Risk Based Quality Management Data MonitorApply →Fresh
Feb 3 $116,000 - $155,000
Research Triangle Park, NCAbout This Role As a Principal Risk Based Quality Management Data Monitor, you will play a critical role in shaping how clinical trial data is monitored, protected, and elevated to the highest quality standards. You will be at the forefront of implementing Risk-Based Quality Management (RBQM) strategies—ensuring patient safety, regulatory compliance, and data integrity across all phases of clinical research. You’ll collaborate closely with biostatistics, data science, safety/pharmacovigilance, clinical operations, and vendors to detect and triage signals early, optimize KRIs/QTLs, and drive continuous process and technology improvements across the portfolio. This position is ideal for someone who thrives on analytical... | |
Distinguished Scientist, Clinical Research, Thoracic MalignanciesFresh
Feb 3 $310,900 - $489,400 USA - New Jersey - Rahway Apply →Distinguished Scientist, Clinical Research, Thoracic MalignanciesApply →Fresh
Feb 3 $310,900 - $489,400
USA - New Jersey - RahwayOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs 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 Distinguished Scientist (Executive Director) and Product Development Team (PDT) Lead, Oncology Global Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology Clinical Research group and in the field of Thoracic Oncology. The Executive Director, PDT Lead will manage the entire cycle... | |
Clinical Project CoordinatorFresh
Feb 3 $85,600 - $156,000 United States - California - Alameda Apply →Clinical Project CoordinatorApply →Fresh
Feb 3 $85,600 - $156,000
United States - California - AlamedaClinical Project Coordinator The Clinical Project Coordinator contributes to the coordination and execution of externally sponsored research projects. The role bridges scientific and operational functions, ensuring that project deliverables align with organizational objectives while maintaining compliance with internal standards and external regulations. operational, and strategic objectives. This is an onsite opportunity in Alameda, CA. What You’ll Work On Assist in planning, coordinating, and monitoring research project activities, including timelines, deliverables, and risk management. Support the preparation, review, and organization of scientific content such as study protocols, abstracts, presentations, and manuscripts. Facilitate communication across cross-functional teams (scientific, clinical, regulatory, and... | |
VP, Clinical Research Head, Nephrology Therapeutic AreaFeb 2 $309,750 - $516,250 USA - Massachusetts - Waltham Apply →VP, Clinical Research Head, Nephrology Therapeutic AreaApply →Feb 2 $309,750 - $516,250
USA - Massachusetts - WalthamGSK seeks an outstanding leader in clinical development to join as VP Clinical Research Head (CRH), Nephrology within the Advanced Portfolio Unit. The Advanced Portfolio Unit works within the Respiratory, Immunology and Inflammation Research Unit (RIIRU). This represents a critical and senior role at GSK, with an opportunity to provide leadership across the full discovery and development lifecycle of our nephrology portfolio. This will require close partnering with leaders from within RIIRU as well as key cross functional partners across the organization. As an individual with significant translational and clinical expertise, you will also be required to operate across the... | |
Senior Coordinator, Clinical SupplyFeb 2 $64,000 - $122,000 North Chicago, IL, United States Apply →Senior Coordinator, Clinical SupplyApply →Feb 2 $64,000 - $122,000
North Chicago, IL, United StatesServes as a primary contract for project management of key Clinical Supply Chain documentation, tasks, and packaging activities in a GMP environment. Owns and supports readiness activities for clinical supply packaging operations. Owns inventory management system set up activities required to drive clinical supply packaging operations. Responsibilities Ensures system set up components are available on time to support Clinical Packaging Production as needed. Owns design, creation, and approval processes for inventory management system activities Identify and lead opportunities for process improvements within and cross functions. Responsible for creating and maintaining processes and procedures related to group activities. Extract job specific... | |
POSITION SUMMARY Assists in analyzing specimens and maintains equipment in good operating condition. 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 timely manner. Ensures all case samples are processed and accounted for Assists supervisor in completing side projects assigned by the manager ... | |
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 position... | |
Test Coordinator Supervisor - Remote Position The Supervisor for the Test Coordination Team will be responsible for leading and supporting a team of Test Coordinators, ensuring excellence in patient care coordination, phlebotomy services, and administrative operations. This role focuses on day-to-day team management, operational efficiency, compliance, and the development of team members. The Supervisor acts as the primary escalation point for internal and external queries, supporting seamless collaboration between field teams, patients, and operational departments. This position requires strong organizational, leadership, and communication skills, and will include up to 50 % travel to support staff coverage, audits, and... | |
Farm Coordinator Intern, Monday-Friday, 7:00am-3:30pm - Summer 2026Feb 2 $35,000 - $56,000 US - WI - Madison Apply →Farm Coordinator Intern, Monday-Friday, 7:00am-3:30pm - Summer 2026Apply →Feb 2 $35,000 - $56,000
US - WI - MadisonHelp 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 The Farm Specialist Intern will help operate Exact Sciences’ onsite hydroponic farms. Operation includes seeding, transplanting, and harvesting as well as cleaning and maintenance tasks to ensure proper and safe food handling and growing in the farm. Essential... | |
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. The Clinical Research Director (CRD), Immunology & Inflammation (I&I) Therapeutic Area is responsible for the creation of the clinical development plan in alignment with the project strategy, its endorsement by governance and its execution in close collaboration with clinical operations. The CRD is expected to advance scientific and clinical knowledge for immunology in Gastroenterology, incorporate new methodologies and pro-actively progress study execution. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to... | |
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. Reporting to the Global Project Head, the CRD leads clinical trial strategy of assigned program(s) within the clinical development team, including interactions with Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish the development strategy and execute the development plan. The clinical development team further develops a compound through life cycle management. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and... | |
Senior Medical Research CoordinatorFeb 2 $68,000 - $136,000 United States - Illinois - Lake Forest Apply →Senior Medical Research CoordinatorApply →Feb 2 $68,000 - $136,000
United States - Illinois - Lake ForestThis position works out of our Lake Forest, IL location in the diagnostics division. The Senior Medical Research Coordinator will manage and coordinate the scientific studies between Abbott and the broader external key opinion community. Overall, this role will maintain and drive the Core Medical Global Strategy in scientific research for one of Abbotts most dynamic and active divisions. What You’ll Work On Responsible for compliance with applicable Corporate and Divisional Policies and Procedures. Prepare, coordinate, and implement agreements that maximize the collaborative experience and support Medical and Scientific activities on time and in budget. Responsible for timely communication of... | |
Sr. Clinical Trial Physician, NeuropsychiatryFeb 2 $308,700 - $374,075; $275,630 - $333,998 Cambridge Crossing - MA - US Apply →Sr. Clinical Trial Physician, NeuropsychiatryApply →Feb 2 $308,700 - $374,075; $275,630 - $333,998
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 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 high performing Study Delivery... | |
Director, Early Precision Medicine Regulatory AffairsJan 30 $244,110 - $295,806; $217,960 - $264,113 Princeton - NJ - US Apply →Director, Early Precision Medicine Regulatory AffairsApply →Jan 30 $244,110 - $295,806; $217,960 - $264,113
Princeton - NJ - USThe Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for biomarkers and diagnostics, focusing on early-stage development through proof of concept and supporting registrations. This role establishes scalable frameworks for investigational assay development, ensuring timely, compliant submissions that support patient stratification in Phase I/II studies. As a key member of the Translational Medicine CLIA Laboratory Steering Committee, the director drives coordinated early-stage drug-diagnostic strategies and health authority engagement to accelerate access to precision therapies. The position demands deep scientific and regulatory expertise (US, EU, Canada, PMD, TGA or Global Devices/IVD preferred), cross-functional leadership, and a commitment to... | |
Coordinate and distribute work in assigned area. Establish priorities to optimize the weighing rooms turnaround. Oversee the drug weighing operation to ensure full GMP (Good Manufacturing Practice) compliance. Request materials and adjust inventories needed for production. Responsibilities List up to 10 main responsibilities for the job. Include information about the accountability and scope. Assign personnel to weigh materials needed. This includes allocation/de-assignment of materials and being able to release orders. Assigns, verifies, and completes documentation for material handling. Use the inventory controls and transaction systems (POMSnet and/or SAP system) to create and confirm orders, adjust inventory and consume materials ensuring... | |
Senior Principal Scientist, Clinical Research, Endometrial CancerJan 30 $282,200 - $444,200 USA - Pennsylvania - North Wales (Upper Gwynedd) Apply →Senior Principal Scientist, Clinical Research, Endometrial CancerApply →Jan 30 $282,200 - $444,200
USA - Pennsylvania - North Wales (Upper Gwynedd)The Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area. Our company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Clinical Director may manage the entire cycle of clinical development for their assigned studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Role Responsibilities Specifically, the Senior Clinical Director may be responsible for Evaluating pre-clinical and translational work for the purpose of generating early clinical development plans and Investigational New Drug applications Developing clinical development... | |
Director, Clinical Research, Cardiovascular and RespiratoryJan 30 $255,800 - $402,700 USA - New Jersey - Rahway Apply →Director, Clinical Research, Cardiovascular and RespiratoryApply →Jan 30 $255,800 - $402,700
USA - New Jersey - RahwayThe Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the [insert name of TA ] therapeutic area. Our company's [insert name of TA] medicines span all phases of clinical development (pre-clinical to post-licensure). The Clinical Director may manage the entire cycle of clinical development for their assigned studies including study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. Role Responsibilities Specifically, the Clinical Director may be responsible for Planning clinical trials (designing, collaborating on operational plans, etc.) based on the clinical development strategy Medical oversight and overall... | |
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... | |
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. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main Responsibilities The role of the Senior CRD is to Act as a mentor for... | |
Containment Specialist & Capital Projects Coordinator – LRL HSEJan 29 $65,250 - $169,400 US, Indianapolis IN Apply →Containment Specialist & Capital Projects Coordinator – LRL HSEApply →Jan 29 $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. Containment Specialist & Capital Projects Coordinator – LRL HSE Job... | |
Manager - Kenosha County Security CoordinatorJan 29 $65,250 - $171,600 US, Pleasant Prairie WI Apply →Manager - Kenosha County Security CoordinatorApply →Jan 29 $65,250 - $171,600
US, Pleasant Prairie WIAt 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 Kenosha County Security Coordinator will join the Utilities, Facilities, and... | |
Senior Director, Clinical ResearchApply →Jan 28 $270,000 - $294,500
Jersey City, NJPosition We are seeking a physician with a strong clinical background and a passion for drug development to join our Clinical Development team to serve as a Study Responsible Physician, Senior Director, Clinical Research. In this role, you will play a pivotal part in advancing our oncology and/or non-oncology pipeline by providing medical expertise, leadership, and operational oversight for a clinical development study(ies). About You You are a highly accomplished professional who excels in the development and execution of clinical projects. As a key member of the cross-functional Development Teams and the Clinical Study Teams, you will employ your expertise... | |
Clinical Research Associate II- Shockwave MedicalJan 28 $87,000 - $140,300 Santa Clara, California, United States of America Apply →Clinical Research Associate II- Shockwave MedicalApply →Jan 28 $87,000 - $140,300
Santa Clara, California, United States of AmericaJohnson & Johnson is hiring for a Clinical Research Associate II– Shockwave Medica l to join our team. The position is FULLY REMOTE and can sit anywhere in the US. 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... | |
Clinical Research Associate II- Shockwave MedicalJan 28 $87,000 - $140,300 Santa Clara, California, United States of America Apply →Clinical Research Associate II- Shockwave MedicalApply →Jan 28 $87,000 - $140,300
Santa Clara, California, United States of AmericaJohnson & Johnson is hiring for a Clinical Research Associate II– Shockwave Medica l to join our team. The position is FULLY REMOTE and can sit anywhere in the US. 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... | |
Intake Coordinator I Oncology – Customer SupportJan 28 Salary N/A Phoenix - CC17 Apply →Intake Coordinator I Oncology – Customer SupportApply →Jan 28 Salary N/A
Phoenix - CC17At 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... | |
Quality Systems Document Coordinator Day Shift, Casa Grande, AZJan 28 $19 - $38 United States - Arizona - Casa Grande Apply →Quality Systems Document Coordinator Day Shift, Casa Grande, AZApply →Jan 28 $19 - $38
United States - Arizona - Casa GrandeQuality Systems Document Coordinator Join our Quality Assurance team as a Quality Systems Document Coordinator, where you will play a key role in maintaining document integrity, supporting regulatory compliance, and ensuring the accuracy of quality‑related processes across the plant. This position works out of our Casa Grande, Arizona 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® –... | |
Project Coordinator - 1st Shift - New Altavista WarehouseJan 28 $21 - $42 United States - Virginia - Altavista Apply →Project Coordinator - 1st Shift - New Altavista WarehouseApply →Jan 28 $21 - $42
United States - Virginia - AltavistaThis position works out of our new Altavista, VA 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. Altavista, Va. , is one of Abbott’s largest nutrition manufacturing plants equipped with advanced technology to ensure efficient production. Working here will make you feel like you’re... | |
Principal Scientist, Clinical Research, ImmunologyJan 27 $250,800 - $394,800 USA - New Jersey - Rahway Apply →Principal Scientist, Clinical Research, ImmunologyApply →Jan 27 $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... | |
Administrative Coordinator, US CVRM Do you have expertise in executive administration support, and passion for communication and collaboration? Would you like to apply your expertise to impact the US Cardiovascular Renal Metabolic (CVRM) Biopharmaceuticals Commercial Team s in a company that follows the science and turns ideas into life changing medicines? Then AstraZeneca might be the one for you! At AstraZeneca we turn ideas into life changing medicines. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. We are focused on the potential of science to address the unmet needs of patients around... | |
Administrative Coordinator - R&D Client Facing TechnologyJan 26 $71,347 - $92,501 US - California - Thousand Oaks Apply →Administrative Coordinator - R&D Client Facing TechnologyApply →Jan 26 $71,347 - $92,501
US - California - Thousand OaksAdministrative Coordinator – Client Facing Technology - Research & Development What you will do In this vital role, you will provide administrative support to the Associate Vice President, Client Facing Technology Research & Development. You’ll join a collaborative Client Facing Technology organization focused on delivering business critical digital solutions to support Amgen’s mission. This is a hybrid/flexible commuter role based in Thousand Oaks, CA. Managing complex calendars and scheduling meetings across global time zones. Coordinating domestic and international travel, including expense reporting via Concur. Supporting Leadership Team meetings and Townhalls. Supporting department operations, including onboarding and offboarding, technology setup,... | |
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. The Clinical Research Director (CRD), Rare Diseases Therapeutic Area, is responsible for creation and execution of the clinical development strategy for assigned projects/studies in this Therapeutic Area (TA). The CRD is responsible for the creation of the clinical development plan in alignment with the project strategy, its endorsement by governance and its execution in close collaboration with clinical operations. The CRD is expected to advance scientific and clinical knowledge and lead clinical... | |
Sr. Clinical Lab Scientist, AnalyticalJan 26 $69,000 - $122,000 US - WI - Madison Apply →Sr. Clinical Lab Scientist, AnalyticalApply →Jan 26 $69,000 - $122,000
US - WI - MadisonHelp 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 The Senior Clinical Laboratory Scientist will be responsible for performing moderate and high complexity laboratory testing on patient specimens, interpreting and reporting patient results, performing quality control and quality assurance procedures, assisting Laboratory Leadership with advanced laboratory duties,... | |
Clinical Trial Application Lead, Biogen West Coast HubJan 26 $118,000 - $158,000 San Francisco, CA Apply →Clinical Trial Application Lead, Biogen West Coast HubApply →Jan 26 $118,000 - $158,000
San Francisco, CAAbout This Role As the Regulatory Manager, Clinical Trial Application (CTA) Lead, you will play a key role in supporting the planning and execution of clinical trial application activities across global studies. You will collaborate closely with Clinical Research Organizations (CROs) and internal stakeholders such as study management teams to ensure timely and compliant study startup and maintenance. You must have experience with clinical trial applications, particularly in the EU to be successful in this role. The Regulatory Manager will report to the Head of Clinical Trials Application, within Biogen’s Global Regulatory Affairs organization. This is a hybrid role based... | |
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. Sanofi's Biomarkers & Precision Medicine group, within the Translational Medicine Unit, seeks an experienced Biomarker and Precision Medicine Lead. This data-driven position focuses on leading the development and implementation of decision enabling translational medicine strategies for our robust pipeline in Immunology and Inflammation with a specific focus on our growing pipeline in Inflammatory Bowel Disease (IBD). The role is critical in identifying and validating biomarkers that predict patient response, demonstrate molecular activity... | |
Clinical Research Associate (CRA), Oncology, As a Field Based Clinical Research Associate , you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives. In this role as an Oncology CRA , you will have the local responsibility for the delivery of the studies at allocated centers and are active participants in the local study team(s). You’ll work in close collaboration with other Monitors and the Local Study Delivery Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner. You will also be responsible for... | |
Gap Closure Program Operations CoordinatorJan 23 $76,000 - $125,000 US - WI - Madison Apply →Gap Closure Program Operations CoordinatorApply →Jan 23 $76,000 - $125,000
US - WI - MadisonHelp 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 The Operations Coordinator supports a working leader (Associate Director, Operations) within the Market Access Gap Closure Program by coordinating, executing, and communicating cross-functional initiatives that directly impact client experience and operational outcomes. This role functions as a project-management-style... | |