- 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 (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
- 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
- IQVIA (Parsippany, NJ)
- …- Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws, ... **Position Specifics** This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout.… more
- Pfizer (Peapack, NJ)
- **Position Summary** You will provide scientific oversight and support data integrity and quality of clinical trial(s) in support of the development strategy for ... program. + Responsible for scientific oversight, data integrity and quality of the clinical trial(s). + Authors...the side of the sponsor. + Strong knowledge of clinical procedures, ICH guidelines, GCP and familiarity… 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
- Bristol Myers Squibb (Princeton, NJ)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Senior Medical Director - Clinical Development (GU Cancer/Prostate Renal) has ... GU cancers. This role provides medical direction and high quality scientific and clinical knowledge to lead...and standard operating procedures (SOP's). + Solid understanding of GCP and ICH guidelines. **Physical demands** While performing the… more
- Deloitte (Morristown, NJ)
- Senior Data Scientist, Specialist Senior - SFL Scientific Our Deloitte Strategy & Transactions team helps guide clients through their most critical moments and ... in building industry-specific, artificial intelligence (AI) technologies. We are hiring a Senior Data Scientist to collaborate directly with clients to design and… more
- Bristol Myers Squibb (Princeton, NJ)
- …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Senior Manager, AI Innovation and Excellence, is a key hands-on leader ... to execute and deliver AI/ML solution while collaborating closely with senior management for guidance and supervision, and collaborating closely with business… more