Clinical Operations Jobs in Pharma & Biotech

The Administrative Coordinator, FP&A role supports to two Vice Presidents, acting as an enabler and force multiplier for these leaders. Key Responsibilities Collaboration Builds trusting relationships and flexes working style to effectively collaborate across teams and levels to drive outcomes Confidentiality Maintains strict confidentiality of sensitive and non-public information (e.g., personnel data, business plans, financial information, and executive communications) in accordance with company confidentiality policies. Detail‑Oriented Demonstrates a high level of accuracy and attention to detail across all work. Ensures information, schedules, logistics, and deliverables are complete, precise, and thoughtfully reviewed. In‑Office Presence & Engagement Maintains a consistent in‑office presence...

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...

Responsibilities Log shipments and receive samples for clinical and/or toxicology trials, in accordance with priority set by Bioanalysis team Notify manager and sample “owner” of any abnormal receipt conditions for follow up with site/vendor that incorrectly shipped samples Work with vendor/site/clinical to resolve any sample discrepancies as necessary Ensure that alarms from the temperature monitoring system are addressed within expected timeframes Manage sample storage volumes and the sample lifecycle management process to ensure the timely transfer and/or disposal of eligible samples Assist with the development of trial-specific CLW as needed Act as administrator to the temperature monitoring system and manage...

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, provides contextual information on the clinical trials, connects stakeholder to the investigative sites and strengthens AbbVie’s...

POSITION SUMMARY Assists in analyzing specimens and maintains equipment in good operating condition. PRIMARY RESPONSIBILITIES Assist in testing of patient samples according to standard operating procedure. Meet expected performance metrics within role as applicable. Responsible for maintaining updated understanding and knowledge of methods performed in the lab Provide guidance for new team members. Follows GLP (good laboratory practice) maintain clean and organized workspace Completes training and other deadlines on time. Recognizes, escalates, and troubleshoot equipment malfunctions and common processing errors according to the laboratory’s standard operating procedures Recognizes, documents, and escalates...

POSITION SUMMARY TheSenior Clinical Research Associateis responsible for the overall operational execution of clinical studies on one or more clinical projects/programs; from study concept through study completion. This position will perform required job duties with guidance from Clinical Trial Managers to ensure that trial timelines, costs, and quality metrics are met, and the study is conducted in compliance with the study protocol, SOPs, and applicable regulatory requirements helps design and execute clinical research activities. PRIMARY RESPONSIBILITIES Provide high level logistical support for clinical study operations, including study start up, study supplies, site qualification, site initiation, site management, study monitoring,...

Principal Scientist (Director) in Translational Medicine-Oncology Translational Medicine at our Research Division is responsible for early clinical development of novel therapeutics, working in close collaboration with Discovery Sciences and late-stage Clinical Research. We work with all therapeutic areas within our Research Division. We are seeking a highly qualified individual for a position in our group. Candidates must have a strong background in basic and/or clinical translational research and a desire to work collaboratively across different therapeutic areas. Translational Medicine is specifically responsible for Leadership of the early clinical development strategy for novel therapy programs from Preclinical Candidate approval through Clinical...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS Texas, Illinois, Indiana, Ohio, Tennessee Ophthalmology experience required. The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS Texas, Illinois, Arizona, Florida, California, NY, Colorado The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding and developing new...

IRT Senior Coordinator is responsible for providing end-to-end IRT (Interactive Response Technology) systems project management support including, but not limited to, gathering study-specific user requirements, executing UAT tasks, managing project timelines, managing and enforcing IRT systems Standards. IRT Sr. Coordinator also monitors system change requests and acts as our Company’s IRT systems subject matter expert while liaising with external vendors. Accountable for making decisions regarding IRT process, issue resolution, and deviations from standards. Applies IRT systems expertise on day-to-day activities when issues are escalated. Communicates with internal and external stakeholders and escalates risks. May participate and lead in process improvement...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS Illinois, Colorado, South Florida, New York, California, Houston, Dallas The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding and developing...

The Manager, Trial Supply Management executes supply strategies for all investigational product based on the scientific and regulatory confines of the drug’s development with minimal supervision. Key Responsibilities Collaborates with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers, including but not limited to Global Drug Development, Pharmaceutical Development, Product Development Quality (PDQ), External Vendors and Medical to ensure all needs are met. Partners with the Clinical Supply Lead (CSL) in planning and communicating the clinical supply chain strategy in support of global clinical studies to promote optimal use and alignment with study and corporate goals....

Senior Administrative Coordinator, Cell Therapy Technical Operations (CTTO) Location Gaithersburg, MD Introduction to the Role Are you ready to orchestrate a senior executive’s priorities and help accelerate transformative cell therapies to patients? Do you thrive in fast-moving environments where organization, judgment, and anticipation help leaders achieve more? Based in Gaithersburg, MD, you will partner directly with the Vice President and Head of Cell Therapy Technical Operations. You will manage complex calendars, global stakeholders, and critical governance activities, helping the team reduce friction, uphold quality and safety, and move at pace. This role requires presence, poise, and persistence. You will work...

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at We are searching for the best talent for Manager, Trial Delivery Management (TDM) to be located in one of the following locations (Hybrid). (Remote working will be considered on a case by case basis and with approval of the business). High Wycombe...

We anticipate the application window for this opening will close on - 18 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life We are seeking a committed professional to...

As the Biomarker and Precision Medicine Lead, you’ll be developing and implementing translational medicine strategies for our robust pipeline in Immunology & Inflammation. Ready to get started? 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 The Biomarkers & Precision Medicine group at Sanofi, within the Translational Medicine Unit, seeks an experienced Biomarker and Precision Medicine Lead. This position focuses on developing and implementing translational medicine strategies for our robust pipeline in Immunology & Inflammation. The role is critical...

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...

About MedTech Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Your unique talents will help patients on their journey to wellness. Learn more at We are searching for the best talent for OEM Coordinator . You will be responsible for Process service activities within the S&R platform software for service and complaints to capture results and activities performed. Document results of service and/or test operations on data sheets and service records. Perform processing duties for OEM devices to be serviced including activities but not limited to...

2nd shift 1pm -930pm Monday - Friday Responsibilities Transfer finished goods inventory from manufacturing and Receiving to warehouse locations for order fulfillment Monitor and segregate finished goods inventory that are placed on hold daily Facilitate transfer requests to and from offsite storage by generating reports through ERP Perform cycle counts, reconcile inventory variances and submit for completion Reconcile inventory discrepancies by investigation prompted by customer service inquiry and SFDC reports Perform random location audits for inventory accuracy and maintenance Monitor and account for inventory in temporary transit locations to ensure proper inventory transfer is completed Generate reports and complete special...

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...

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...

Location On-Site in Boulder, CO (Foresight Dx business unit, a Natera company) Foresight Diagnostics is a molecular diagnostics company pioneering non-invasive cancer detection through highly sensitive, cell-free DNA-based liquid biopsy technologies. Our proprietary methods - originally developed at Stanford University - are designed to detect smaller tumors earlier and enable more personalized treatment strategies for patients with cancer. We sit at the intersection of molecular biology, bioinformatics, and next-generation sequencing (NGS), and we translate rigorous science into clinically meaningful solutions. Following our acquisition by Natera, we now combine the agility of a mission-driven startup with the scale and resources of...

The Safety Clinical Research Associate (CRA) is responsible for supporting clinical safety and medical affairs activities through the collection, review, preparation, and management of clinical safety documentation and operational processes. The role provides critical support for safety committees, case narratives, source document management, translation coordination, and regulatory inspection readiness while ensuring compliance with applicable procedures and regulatory requirements. This new team member will work on-site at our Maple Grove, MN location. What You’ll Work On Safety Documentation and Source Record Management Collect, track, review, and manage source documentation associated with adverse events, serious adverse events, complaints, and clinical investigations. Ensure...

#LI-Hybrid Position Location Cambridge, MA We are Clinical Sciences and Innovation at Novartis. A dynamic group of Clinical Trial Leaders (Clinical Scientists) who plan and execute early phase trials worldwide. From First-in-Human to ph2a studies and beyond. We design and operationalize trials, ensuring they run smoothly, on time and – most importantly – with patients’ interests to the fore. Curious, unbossed and inspired; we are committed to flexibility in the workplace. As a member of our team, you will support or lead the clinical science and operations of planning and executing translational medicine clinical trials. Collaborate across our global network....

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding and developing new sites. Participates in internal meetings and workstreams as SME for monitoring processes and Systems. Responsibilities include,...

The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Senior Director has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Responsibilities Specifically, the Senior Director may be responsible for Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy...

Are you ready to lead a high-performing team that accelerates pivotal clinical trials and gets transformative medicines to patients faster? As CRA Manager within US Site Management and Monitoring, you will direct a group of Clinical Research Associates to deliver robust site performance, first-time quality, and on-time execution across a dynamic portfolio. Your leadership will ensure we meet the highest scientific and regulatory standards while keeping patient outcomes at the center. You will shape how we deploy monitoring expertise, optimize resources, and strengthen site relationships across multiple indications. In this role, you will translate strategy into action—coaching, removing barriers, and...

JOB POSITION SUMMARY 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 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....

About This Role As a Clinical Trial Manager, you will be a vital part of the PO&T team within the Implantable Device Unit, supporting the planning, coordination, and execution of clinical studies. Your role is crucial in ensuring that trials are conducted efficiently and in compliance with regulations, driving valuable outcomes for the business. Working closely with cross-functional partners, study sites, and external vendors, you will manage the day-to-day operations of clinical trials, tracking progress and identifying risks. By maintaining trial documentation and collaborating with diverse teams, you will help ensure high-quality data and participant safety. This position offers the...

Johnson & Johnson Vision is recruiting for a Senior Manufacturing Support Coordinator, located in Jacksonville, FL. About 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...

Global Pharmacovigilance Quality Audit & Inspection Readiness Coordinator - VIE Contract Location United States of America, Morristown Target start date 01/12/2026 iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28. PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship. PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide. Therefore, only applications that are submitted in English...

Oncology remains a core therapeutic area at AbbVie, featuring a robust portfolio of marketed products and a promising oncology pipeline. AbbVie is currently seeking a dynamic Medical Director / Scientific Director for Medical Affairs, Precision Medicine, to lead U.S. CDx strategy in oncology. This role requires a strong background in diagnostics, pathology, biomarkers, and cancer therapeutics, as well as a demonstrated commitment to precision medicine. This position must be based at our Mettawa, IL headquarters and will follow a hybrid schedule of 3 days/week in office. Key Responsibilities Lead and deliver a comprehensive, U.S. focused medical strategy for CDx-dependent indications...

AstraZeneca is making one of the boldest investments in Cell Therapy in the industry — building a portfolio that spans autologous, allogeneic, and in vivo modalities with the ambition to bring these transformative treatments to patients around the globe. Every autologous cell therapy begins with a single patient — their cells collected, shipped, engineered, and returned as a living treatment designed specifically for them . The Senior Specialist, Cell Therapy Vein-to-Vein Coordinator is at the center of that orchestration. You will manage active patient and product journeys end-to-end — from slot scheduling and apheresis collection through courier transportation, manufacturing, release,...

Our J&J MedTech Electrophysiology clinical team is currently recruiting for a Clinical Research Leader. This role is located in Irvine, California. 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 by innovation at...

Position Overview The Associate Clinical Experience Analyst- Genetic Counselor Assistant 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 support of the rare disease customer facing team for PreventionGenetics. Shift Monday - Friday, Shift rotates weekly with start times ranging from 700AM-1030AM CST and end times ranging from 330PM-700PM CST. Must be available between the hours of 7AM-7PM CST. Essential Duties Include but are not limited to the following Acts as a clinical liaison...

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,...

Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, we are building a new kind of healthcare company - one that is ready to help create a healthier future for all of us. Our ability to excel depends on the integrity, knowledge, imagination, skill, and teamwork of an individual like you. To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your...

The 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...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS AND BE FLUENT IN SPANISH South Florida - Ft. Lauderdale, Miami, Boca Raton, Key Largo The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands...

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. We are looking for a Senior Clinical Research & Development (CRD) to join our Rheumatology/Transplant clinical development team, playing a pivotal leadership role in shaping and advancing our clinical programs. If you are a medically trained expert with a passion for immunoscience and a drive to mentor, collaborate, and innovate, this is your opportunity to make a meaningful impact at scale. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving...

About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at We are searching for the best talent for a Director Forecasting, Randomization & Trial Supply Management (RTSM) in either Horsham, PA, Titusville, NJ or Beerse, Belgium. In the Clinical Supply Chain (CSC) – Digital Solutions department we drive digital...

About Innovative Medicine Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow. Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way. Learn more at Please note that this role is available across multiple countries and may be posted under different requisition numbers to comply with local requirements. While you are welcome to apply to any or all of the postings, we recommend focusing...

We anticipate the application window for this opening will close on - 18 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life We are seeking a committed professional to...

We anticipate the application window for this opening will close on - 24 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life In this exciting role as a Senior...

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,...

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. Provides high-level administrative and coordination support to an individual manager and to the Regulatory, Safety, and Quality teams based in Parsippany, NJ....

What You Will Do A leadership role combining clinical, scientific, commercial, and operational expertise to drive the successful development and delivery of novel therapeutic approaches for inflammatory myopathies, JIA, and/or Sjogren’s Disease . Responsible for integrating research and development strategies, ensuring robust, commercially viable study designs and execution, and optimizing cross-functional collaboration from early research through to late-stage clinical development and lifecycle management. Typical Accountabilities Integrate the research and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical research professionals, or by supporting such a team as an expert in...

What You Will Do Externally recognized as a thought leader with deep expertise in both clinical research and development with deep understanding of autoimmune disease, specifically inflammatory myopathies, JIA and/or Sjogren’s disease. Knowledge and expertise in cell therapy is a plus . Drive the integrated clinical research and development strategy and execution, to ensure value creation and regulatory/market success through innovative, cross-functional leadership. Operate independently and at scale, influencing both operational excellence and strategic direction at the highest organizational levels. Typical Accountabilities Develop and align strategies and objectives for Clinical Research & Development, ensuring they support AstraZeneca’s global goals...

What You Will Do E xpert in the field of drug research and development, contributing deep specialist knowledge of inflammatory myopathies, JIA and /or Sjogren’s Disease . Operat e with significant independence, i ntegrate advanced scientific, operational, and commercial expertise to guide the full lifecycle of clinical research and development projects. E nsure alignment of scientific and business objectives across multiple functions for drug candidates, actively lead multidisciplinary teams, steer project strategy and execution, and champion process innovation and compliance to deliver high-impact results. Accountabilities Provide specialist scientific and technical expertise for clinical research and development, acting as a...

What You Will Do A leadership role combining scientific, commercial, and operational expertise to drive the successful development and delivery of novel therapeutics for patients with inflammatory myopathies and/or Sjogren’s Disease and autoimmune diseases . Responsible for integrating research and development strategies, ensuring robust, commercially viable study designs and execution, and optimizing cross-functional collaboration from early research through to late-stage clinical development and lifecycle management. Accountabilities Integrate the research , clinical, scientific and commercial aspects of drug development to ensure successful, value creating product development, either by overseeing a team of clinical research professionals, or by supporting such a team...

Our 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...

This position will be located at East Hanover NJ or Tempe, AZ site and will not have the ability to be located remotely. This position will require travel as defined by the business. The Patient Coordinator 1 (PC 1) is responsible for providing support and resolution for customer requests. They accurately and efficiently answer calls that are received from patients, their caregivers, and health care practitioners. The PC1 educates and addresses questions regarding the brand, enrollments, and basic case status updates as appropriate. The PC 1 role will support high volume programs associated with retail and specialty pharmacy products. The...

We anticipate the application window for this opening will close on - 21 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life We are seeking a committed professional to...

The Clinical Lab Technician 1 will be in a regulated Clinical Laboratory receiving, processing, and performing high throughput testing of samples using standard laboratory equipment and robotic liquid handling systems. Responsibilities Perform accessioning of samples including receipt, storage, aliquoting, and disposition Perform the SomaScan assay using robotic liquid handling systems and other laboratory equipment Perform tasks per established Standard Operating Procedures (SOP) and Work Instructions (WI) Ensure accurate and timely results Maintain sample integrity and traceability throughout sample processing Adhere to Good Documentation Practices (GDP) Comply with laboratory safety policies and procedures Comply with Quality Assurance and Regulatory requirements Participate...

Clinical 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...

Responsibilities Picking of materials using RF scanners in ambient, refrigerated and frozen storage locations based off of shipping pick lists provided Packing of materials according to procedure which includes handling of packing supplies, corrugated boxes, coolers, cold packs and dry ice Generating shipping labels through ERP and carrier software Performing Area Line Clearance to ensure quality of each shipment and completing documentation following Good Documentation Practice Maintaining organization of work areas through 6S (sort, straighten, standardize, shine, sustain, safety) Support other warehouse and logistic tasks as assigned which can include Receipt of incoming goods (stock and non-stock), labeling and stocking...

Clinical Research Associate II The CRA II will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards. This position will be based in our Alameda, CA office. What You’ll Work On Conduct single or multi-center medical device clinical studies. Perform study site visits (SQV, SIV, IMV, COV), generate monitoring trip reports, and track resolution of action items. Participate in study start up activities. Responsible for shipping study devices and supplies to...

This position is responsible for providing Quality support for access management of a document control system. What You’ll Work On Process documentation system access requests and ensures timely completion in accordance with established procedures. Review requests for completeness, accuracy, approvals, and compliance requirements. Grant, modify, and remove user access within documentation and quality management systems. Provide customer support and guidance regarding access-related inquiries and requests. Troubleshoot and resolve documentation system access issues and incidents. Maintain accurate records and documentation of access management activities. Support audits, inspections, and periodic access reviews. Drive continuous improvement initiatives to enhance process efficiency and customer...

This position works out of our Abbott Park, IL location within the CHR Corporate Human Resources division. 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,...

The TAIP TA Lead is a senior leadership role reporting directly to the Head of the TAIP unit within Bristol Myers Squibb’s Trial Analytics, Insights, and Planning (TAIP) organization—an internal consulting team that drives clinical development excellence through data-driven insights, feasibility modelling, and strategic trial planning. As the analytics lead for the Oncology therapeutic area (TA), you will be accountable for the end-to-end analytics strategy and execution across a global portfolio of clinical trials within that TA—supporting trial-level planning, overseeing delivery performance, and leading a team of analytics professionals across multiple levels and geographies. This role will have direct reports...

When you join BMS, you are joining a high-achieving team united by a common mission. The Informatics and Predictive Sciences (IPS) mission is to Pioneer, Partner and Predict to drive transformative insights for patient benefit. IPS conducts applied computational research in areas that include genomic, structural and molecular informatics, computational and systems biology, patient selection and translational biomarker research, and broader fields including knowledge science, epidemiology and machine learning—across the full lifecycle of drug discovery and development and across all therapeutic areas at BMS. We do this in close partnership with scientific and clinical experts in the field, both inside...

The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Cardiovascular and Respiratory therapeutic area. Our company's cardiovascular and respiratory 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. 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 conduct of ongoing or new...

Position As a Senior Clinical Trial Manager, you will play a pivotal role in leading and overseeing our global clinical trial operations. Operating in a dynamic and collaborative environment, you will provide strategic direction and hands-on management to ensure the successful execution of global clinical trials in multiple regions, contributing to the development of groundbreaking therapies with the potential to transform patient lives. The successful candidate will need minimal oversight, will work closely with cross-functional teams to ensure successful completion of studies within timelines and budget, with a focus on exquisite quality to support excellence and world class clinical study...

Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative therapies for patients with devastating diseases. Our next-generation genome-editing technology enables superior precision to develop cell therapies that are armored to potentially improve activity against diseases. We believe the future of cell therapy is off-the-shelf, and we are advancing our pipeline of off-the-shelf, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases. Members of the Caribou herd open their minds to new ideas and welcome diverse perspectives. We proudly assert that teams do...

We are searching for the best talent for a Senior Field Research Specialist for the J&J MedTech Interatrial Shunting business in the US. 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...

Make the most meaningful impact of your career in this rewarding role with Biogen, a well-established pioneer in the pharmaceutical industry. This is your rare opportunity to transcend day-to-day management operations as you design operational strategy and oversee our clinical research organization (CRO) partners to develop clear protocol concepts and final protocols. The best part You will own responsibility for entire clinical trial studies, including operational design, successful delivery, and the positive impact on the lives of patients with a wide array of neurological conditions, including nephrotic conditions, multiple sclerosis (MS), Alzheimer’s disease, and spinal muscular atrophy (SMA). Working from...

Administrative Coordinator – DATA What you will do The Administrative Coordinator (AC) will be primarily responsible for complex administrative support activities, working as part of a global administrative team supporting Associate VPs, Executive Directors, and other staff located in San Francisco, Thousand Oaks, Boston and other remote sites within Discovery Sciences, Advanced Technologies, & AI (DATA). Key Responsibilities Participate as an active team member, working both independently and in cooperation with other team members, to complete projects and assignments in a timely manner Manage multiple priorities in a fast-paced, continually changing environment Provide site-based support for meeting management, expenses,...

The Executive Director (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Atherosclerosis section of the Atherosclerosis & Metabolism therapeutic area. The Executive Director will manage and oversee the entire cycle of late stage clinical development from Phase 2 to Phase V, including development of program strategy and design, protocol authoring, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international meeting. She/he will lead cross-functional product development teams that oversee program strategy and execution, will provide internal scientific leadership for cross-functional areas supporting clinical...

We anticipate the application window for this opening will close on - 18 Aug 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life The Senior Principal Clinical Research Specialist –...

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,...

PRIMARY RESPONSIBILITIES Maintain personnel records ensuring compliance of all personnel documentation. Manage onboarding for new employees including new hire orientation. Coordinate compliance of various state and federal requirements including I-9 authorizations. Solicit new/ current employees for diploma/ certification information. Assist in providing support to employees by responding to questions and escalating issues as necessary. Assist with employee communications, including compensation and severance letters. Make employee changes related to compensation, department, manager, shifts etc. in HRIS and coordinate with payroll. Respond to requests for employment verifications and unemployment claims. Assist in maintaining HRIS data, with high degree of accuracy and...

The Early Clinical Scientist (ECS) coordinates the design, planning and execution of early phase clinical trials with the Clinical Director, and internal/external team members. Oversees trials within and/or across program(s)/therapeutic areas and ensures excellence in execution/compliance to support study objectives and data validity. Manages internal/external team performance to achieve project objectives and resolves project performance issues if they arise. Ensures appropriate clinical safety assessment and risk management of compounds. Conducts real-time oversight of ongoing trials to identify and mitigate patient, study design, data or study conduct issues. Reviews and interprets clinical trial data. May conduct on-site study monitoring, including site...

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 site management activities, ensuring compliance...

This position works out of our Alameda, CA location in the Diabetes Care division where we're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. As the Clinical Research Associate II, you will assist in the clinical execution and management of assigned clinical studies. This includes but is not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards. You will also present clinical study opportunities...

The 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. This is a 40 hour a week role with regular work hours between 7 AM and 6 PM. What You’ll Work On Manage key steps in...

The Opportunity This position works out of our Alameda, CA location in the Diabetes Care division where we're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We’re revolutionizing the way people monitor their glucose levels with our new sensing technology. As the Clinical Research Associate I you will assist in the clinical execution and management of all aspects of assigned clinical studies. This includes but not limited to planning and implementation of clinical studies from concept to clinical study report per timelines and quality standards. What You’ll Work...

Johnson & Johnson MedTech, Neurovascular, is recruiting an Associate Director, Clinical Research, to join our team. 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 Please note that this role is available across...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS ALABAMA, GEORGIA, COLORADO, MASSACHUSETTS, MICHIGAN, MARYLAND, PENNSYLVANIA The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding and developing...

CANDIDATE MUST RESIDE IN ONE OF THE FOLLOWING LOCATIONS NEW YORK, NEW JERSEY, TEXAS, CHICAGO, SOUTHERN CALIFORNIA, MISSOURI The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA-Manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as primary site contact and site manager throughout all phases of a clinical research study, taking overall responsibility of allocated sites. Actively develops and expands the territory for clinical research, finding...

The 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 & Metaboslim 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 Planning clinical trials (design, operational plans, settings) based on these clinical development strategies Monitoring and managing the...

We are seeking an experienced Administrative Coordinator to support one of our key Vice Presidents within Global Respiratory and the Immunology team as part of the Biopharmaceutical Business Unit. The primary responsibility is for performing a variety of secretarial and project-oriented activities such as- complex calendar management, travel arrangements, event planning, vendor engagement and all executive level support activities. Specific accountabilities for budget management is also key. Key Responsibilities Executive Representation Respond on behalf of the Vice President to a variety of internal and external stakeholders, ensuring professionalism and effectively managing conflicting priorities. Inquiry Management Handle complex or escalated inquiries...