- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials ... investigator sites to ensure patient safety and quality study...Good Clinical Practices (GCP), and the Sponsor's standards. The Sr . CRA is accountable for site management and monitoring,… more
- Parexel (Trenton, NJ)
- **CRA and Sr CRA positions- Remote - Need for SE Region - FL** **ONCOLOGY preferred** **Job Purpose:** The Clinical Research Associate (CRA) has local responsibility ... data from study sites as per required timelines. + Manages study supplies ( Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site.… more
- Parexel (Trenton, NJ)
- **Job Purpose:** The Senior Clinical Research Associate ( Sr . CRA) is responsible for the site management, site monitoring and close-out of assigned clinical ... trials investigator sites to ensure patient safety and quality study...laws, Good Clinical Practices (GCP), and sponsor standards. The Sr . CRA is accountable for site management and monitoring,… more
- Parexel (Trenton, NJ)
- Join our dynamic Patient Safety team as a ** Senior Physician** where you'll leverage your medical expertise to ensure the safety of patients in clinical trials and ... wellbeing and regulatory compliance. **About the Role** As a ** Senior Physician in Patient Safety** , you'll serve as...provide daily medical support to Parexel staff or site ( investigator /study coordinator), as needed + Review and sign off… more
- Parexel (Trenton, NJ)
- The Senior Clinical Research Associate (SrCRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local ... data from study sites as per required timelines. + Manages study supplies ( Investigator Site File (ISF), etc.), drug supplies and drug accountability at study site.… more
- Parexel (Trenton, NJ)
- **Job Summary:** The Senior Medical Writer will research, create, and edit all documents associated with clinical research. Responsibilities also include: acting as ... to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final… more
- Parexel (Trenton, NJ)
- …with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study teams on TA indication and ... sponsorship as needed with the support of the designated Senior Medical Director/ Global Head of TA (as appropriate)...a Physician in Industry or as a clinical trial investigator with significant clinical research experience The ability to… more
- Bristol Myers Squibb (Princeton, NJ)
- …your application should be directed to Chat with Ripley. R1597474 : Senior Research Investigator , PBPK **Company:** Bristol-Myers Squibb **Req Number:** R1597474 ... **Updated:** 2026-01-06 04:40:29.017 UTC **Location:** Princeton-NJ Bristol Myers Squibb is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender… more
- Taiho Oncology (Princeton, NJ)
- …transforming the landscape of cancer treatment and improving patients' lives. As a Senior Manager, Clinical Research Scientist, you will play a pivotal role in our ... to be at the forefront of cancer research. Position Summary: The Senior Manager, Clinical Research Scientist has responsibility assisting in design, execution and… more
- Norstella (Trenton, NJ)
- Sr . Director/VP/Clinical Delivery Lead, Advisory Services Company: Citeline Location: Remote, United States Date Posted: Nov 4, 2025 Employment Type: Full Time Job ... ID: R-1553 **Description** Sr . Director/VP/Clinical Delivery Lead, Advisory Services **Reports to** :SVP,...industry suppliers, advisors, and investors. Our clients are generally senior -level decision makers in need of support to ensure… more
- Taiho Oncology (Princeton, NJ)
- …and manages complex global studies to support the Clinical Development Plan. The Senior Study Manager (SSM) is responsible for ensuring assigned clinical studies are ... and issues. + Oversee systems to track projects including all study, investigator and ethical review board information, patient recruitment activity, and financial… more
- Philadelphia Insurance Companies (Ewing, NJ)
- …member of Ward's Top 50 and rated A++ by AM Best. We are looking for a Sr . Claims Examiner - SIU to join our team! Summary : Evaluate referred insurance claims for ... investigators conduct appropriate investigations. Review and evaluation of third-party investigator reports for thoroughness and accuracy. Review and evaluation of… more
- Taiho Oncology (Princeton, NJ)
- …relevant clinical documents of high quality, such as study protocol protocol(s), investigator brochure (IB), informed consent forms (ICF), case report forms (CRF), ... the study conduct and operational risks. Represent the molecule at senior management governance meetings. + Co-responsible with Clinical Development, Project… more
- Taiho Oncology (Princeton, NJ)
- …Proposition: Embark on a transformative journey with Taiho Oncology as a Senior Manager, Global Labeling and PV Operations. At the forefront of pharmacovigilance ... on your experience in our rapidly evolving organization. Position Summary: The Senior Manager, Global Labeling Innovation & PV Operations, leads the creation,… more
- IQVIA (Parsippany, NJ)
- …and contribute to process optimization initiatives. + Provide strategic reporting to senior leadership and resolve complex issues with minimal oversight. + **Project ... contact, global cross functional business partners + **Others:** Clinical Investigator Sites, Commercial Suppliers, Clinical Trial Insurance Providers, other… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …amendment, and routine submissions (eg, Development Safety Update Reports / DSURs, Investigator Brochure/ IB updates, etc.). + Leads cross-functional teams in the ... authoring of regulatory documents, including meeting requests, Module 1 documents for original IND, etc. + Provides input to the content of the original label and label updates. + Ensures product packaging and associated information is updated and maintained… more
- Sanofi Group (Bridgewater, NJ)
- …stretch the limits of what you thought was possible. Ready to get started? The Senior Clinical Research Director ( Sr CRD) is noted as the **primary clinical lead ... deliver to multiple operational tasks. The role of the Senior CRD is to: + Act as a mentor...and/or contribute in the the clinical section of the Investigator 's brochure, CTA, IND, DSUR, INDAR, DRMP, RMP +… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Senior Clinical Research Director **Location:** Cambridge, MA or Morristown, NJ **About the Job** Join the engine of Sanofi's mission - where deep ... breakthroughs that could turn the impossible into possible for millions. As the ** Senior Clinical Research Director** ( Senior CRD) within the RARE Therapeutic… more
- Sumitomo Pharma (Trenton, NJ)
- …a dynamic, highly motivated, and experienced individual for the position of Senior Medical Director, Clinical Research (Ophthalmology) to join our R&D Organization. ... writing of clinical study reports + Contributes to the preparation of Investigator Brochures, annual reports, data collection systems and final reports in compliance… more
- Bayer (Trenton, NJ)
- …and diverse minds to make a real difference, there's only one choice.** ** Senior Medical Science Liaison Stroke/Thrombosis New York New Jersey** Senior Medical ... **YOUR TASKS AND RESPONSIBILITIES** The primary responsibilities of this role, Senior Medical Science Liaison, Stroke/Thrombosis are to: **Scientific Expertise** +… more
