- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …safety + Possesses proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or late stage assets; ... components of the Clinical Study Reports with minimal guidance and supports the development of regulatory documents; performs quality review and may approve;… more
- IQVIA (Parsippany, NJ)
- …scientific reports from external sources for inclusion as a resource for content development . + Reviews clinical regulatory documents and comms + Understands ... branding objectives. Primary responsibilities include the management of projects, development of high-quality scientific content, partnering with stakeholders to… more
- J&J Family of Companies (Titusville, NJ)
- …Affairs studies. Supports multi-channel approach of dissemination as well. + Supports Regulatory related activities such as the development of product monographs ... Team. + The TAL will be an expert in medical affairs strategy development taking strong consideration to competitors and overall customer feedback, and will lead… more
- Merck (Rahway, NJ)
- …The Analytical Commercialization Technology (ACT) group within Analytical Chemistry in Development and Supply (ACDS) is seeking applicants for a Senior Scientist ... characterization technologies to drive late-stage small molecule drug product development and commercialization. The Senior Scientist responsibilities include, but… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …operation and maintenance of world-class facilities that enable the discovery, development and delivery of innovative medicines that help patients prevail over ... group, the successful applicant will be primarily responsible for the development of a company-wide approach to perform GLP environmental fate/effects studies… more
- Bristol Myers Squibb (Princeton, NJ)
- …key stakeholders such as Clinical, Medical, Marketing, Market Access, Statistics and Regulatory . **Responsibilities:** + Lead the development of an aligned ... partnerships with external key opinion leaders in clinical, health economics, and outcomes research . **Qualifications:** + A PhD in a related discipline such as… more
- Merck (Rahway, NJ)
- …maintain a strong training program for auditors to ensure their ongoing skills development and ability to detect and communicate GxP compliance concerns + Ensure ... global auditing team + Maintain up-to-date knowledge base with respect to emerging regulatory trends and changes in regulations and standards to incorporate into the… more
- Holtec International (Camden, NJ)
- …requirements, then develop them into mature designs by critical thinking, literature research , interacting with members from other disciplines and vendors, and any ... presentations, and communicate design progress in stakeholder meetings + Support development of engineering and licensing requirements and documentation for nuclear… more
- Bristol Myers Squibb (Princeton, NJ)
- …area scientific & clinical expertise + Familiarity with all phases of drug development , including clinical development , regulatory and life cycle management. ... BMS medicines + Lead the strategic planning and content development of medical advisory boards + Lead the strategic...strategic alignment and scientific rigor of new investigator sponsored research concepts and manage the ongoing ISR portfolio +… more
- Pfizer (Peapack, NJ)
- …integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio. **Position ... contributes to authoring of IBs, site training materials, clinical study reports, regulatory responses, and other clinical and regulatory documents; supports… more