- Bristol Myers Squibb (Madison, NJ)
- …treatment we pioneer. Join us and make a difference. **Position Summary** The RWE Director is a key member of cross-functional teams and RWE-CoE within GBDS. This ... study design using real-world data to facilitate and support development and regulatory interactions of pharmaceutical products. This position is also responsible of… more
- NRG Energy, Inc. (Princeton, NJ)
- …Facebook, Instagram, LinkedIn and X. **Job Summary:** As a member of the Regulatory Compliance NERC Team, the Director NERC Compliance provides essential ... compliance program by conducting periodic audits, gap analyses, and managing program documentation and compliance reporting . With travel to power plant… more
- L'Oreal USA (Clark, NJ)
- …impacts (CIR, RIFM, FDA, ANVISA, Health Canada, and other testing requirements of regulatory agencies). + Define direct reporting team's objectives and ensure ... Home (https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 211205 Director , Skin Product Safety & Toxicology, L'Oreal Research… more
- Parexel (Trenton, NJ)
- …processing for studies including medical review of serious adverse events. * Support regulatory safety reporting activities * Ensure client needs and concerns ... are expanding our esteemed Medical Sciences Team and seeking an Associate/Medical Director to support the growth of our Global Immunology and Inflammation… more
- Bristol Myers Squibb (Trenton, NJ)
- …the overall IH program , there will be a significant focus on biosafety. Reporting to the Executive Director , GPS EHS and S-COE, the Associate Director ... global strategies for industrial hygiene, ensuring alignment with company objectives and regulatory requirements. + ** Program Development & Deployment:** Lead or… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and drug ... drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines,… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …the enterprise. **Key Responsibilities:** + Lead the global EHSS internal audit program , including strategic planning, scoping, execution, and reporting , aligned ... their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary:** The Director , EHSS Audit & Assurance leads the global strategy and execution… more
- Novo Nordisk (Plainsboro, NJ)
- …together to change lives for the better. The Position The Associate Director , Consumer Social Media Strategy is a high-impact, hands-on leadership role responsible ... role translates the corporate digital vision set by the Senior Director into best-in-class digital experiences, driving audience engagement, building brand trust,… more
- J&J Family of Companies (Titusville, NJ)
- …Summary:** We are seeking a highly skilled and motivated **S** **cienti** **fic Director ** to join our RWE team. The successful candidate will apply advanced ... with the Neuroscience Therapeutic Area, Clinical Development, Quantitative Sciences, Regulatory and Patient Reported Outcomes. **Key Responsibilities:** + Design,… more
- Bristol Myers Squibb (Madison, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . Job Description The Associate Director , RBQM - HOCT, ICN will mainly be responsible for developing ... consultation to clinical trials teams throughout study lifecycle. + Provide regulatory intelligence on current and upcoming regulations to ensure we remain… more
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