- Eisai, Inc (Nutley, NJ)
- …on GCP and current regulations for those undertaking clinical studies.Job SummaryThe Associate Director , GCP Quality Assurance works within the ... Global Clinical Quality team to conduct GCP compliance activities at Eisai, at our CROs and...25%)Eisai Salary Transparency Language:The base salary range for the Associate Director , Clinical Quality Assurance… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end ... clinical safety and pharmacovigilance, CROs and other vendors to ensure high quality of laboratory data deliverables to support drug development processes and global… more
- Merck & Co. (Rahway, NJ)
- …a lead GCS Planning program representative) such as clinical development, regulatory, quality and other supply chain areas to negotiate timelines,- strategies and ... - Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. - Preferred Experience and Skills: - - Proficiency… more
- Ascendis Pharma (Princeton, NJ)
- …We offer a dynamic workplace for employees to grow and develop their skills. Associate Director , Global Patient Safety Medical Science reports to Head of GPS ... that all safety reports received from any source are reviewed according to ICH- GCP guidelines, regulatory requirements and company SOPs and procedures. + Performs … more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director , Laboratory Data Management is accountable for the ... clinical safety and pharmacovigilance, CROs and other vendors to ensure high quality of laboratory data deliverables to support drug development processes and global… more
- Bristol Myers Squibb (Princeton, NJ)
- …This position will be based in San Diego, CA or Lawrenceville, NJ. **Summary:** The Associate Director , Clinical Data Management, will play a crucial role in our ... aspects of data management, from planning and coordination to execution and quality control. The successful candidate will be responsible for managing relationships… more
- Merck (Rahway, NJ)
- …a lead GCS Planning program representative) such as clinical development, regulatory, quality and other supply chain areas to negotiate timelines, strategies and ... + Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. **Preferred Experience and Skills:** + Proficiency in using… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …and/o academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 ... and protocols for OPDC products under good clinical practices ( GCP ). This is a remote position. The incumbent will...prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …and academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director is typically ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… more
- Prime Healthcare (Newark, NJ)
- …an award-winning team of dedicated professionals committed to our core values of quality , compassion and community! Saint Michael's Medical Center, a member of Prime ... qualified physicians, nurses, and allied health professionals, the hospital provides top- quality health care services delivered with compassionate care. The first… more
