- Gilead Sciences, Inc. (Parsippany, NJ)
- …global clinical regulations and guidance. + Support the development of GCP Audit material/insights for quality forums and management reviews. _Training & ... and with senior leadership, on key projects and deliveries supporting quality and compliance. + Demonstrates ability to execute against the strategic and… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …position in one of our office locations. Fully remote is not eligible._ The ** Senior Clinical Study Lead** (CSL) is expected to operate with high-degree of ... for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study...study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study… more
- IQVIA (Parsippany, NJ)
- …accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice ( GCP ) and International Conference on Harmonization (ICH) ... in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice ( GCP ) and International Conference on Harmonization (ICH)… more
- Bristol Myers Squibb (Madison, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Scientist reports through the Clinical Science function ... writing, reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing) + Site-facing… more
- Sumitomo Pharma (Trenton, NJ)
- …and communication with cross-functional teams to ensure proper execution and conduct of the clinical trial; generates quality clinical data. + Serves as ... the study team to design, develop and deliver the clinical study to agree upon timelines. + Leads planning...vendors, and ensures the documentations are in accordance with GCP regulatory requirements and consistent with the protocol for… more
- Bristol Myers Squibb (Princeton, NJ)
- …The Senior Manager, Data, Analytics and AI Product Engineer- Clinical Data Management, Global Drug Development Information Technology (GDDIT), Data & Analytics ... BMS. **Key Responsibilities:** + Accountable for delivering strategy, planning, and high- quality technology solutions for Clinical Data Management portfolio. +… more
- J&J Family of Companies (Raritan, NJ)
- …profoundly impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Quality **Job Sub** **Function:** Clinical Quality **Job ... States of America **Job Description:** Johnson & Johnson MedTech Research & Development Quality (RDQ) is recruiting for ** Clinical Supplier Quality … more
- Bausch + Lomb (Trenton, NJ)
- …global team members, other B&L departments (eg, R&D/Project Management, Clinical /Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, ... GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,...purposes. **POSITION REQUIREMENTS** **:** + Strong knowledge of Good Clinical Practices ( GCP ), clinical trials… more
- Bristol Myers Squibb (Princeton, NJ)
- …Read more: careers.bms.com/working-with-us . **Summary:** The position requires an experienced Senior Engineer with a strong focus on cloud native services, AI, ... with expert-level experience in AWS and additional experience in GCP or Azure being a plus. We are looking...Have** + The ideal candidate must be a strong Senior Developer and have experience using AWS services beyond… more
- Actalent (Princeton, NJ)
- We are seeking a dedicated Senior Clinical Project Manager responsible for overseeing the planning, execution, and management of clinical trials across ... study coordinators. + Facilitate collaboration among cross-functional teams including Clinical Operations, Data Management, Medical Writing, Quality Assurance,… more
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