- Merck (Rahway, NJ)
- **Job Description** The Director / Principal Scientist , Regulatory Affairs Liaison, is responsible for the development and implementation of worldwide ... regulatory strategy for their assigned projects in the General...external to GRACS. **Key functions:** + Reports to Senior Principal Scientist (Senior Director ) and/or… more
- Merck (Rahway, NJ)
- …seeking a highly motivated and experienced Anatomic Pathologist (MD) for the role of Principal Scientist ( Director ) to join our innovative team. This ... and advancing digital pathology within our company's clinical therapeutic pipeline. **The** ** Principal Scientist ( Director )** **will have the following… more
- Merck (Rahway, NJ)
- **Job Description** ** Principal Scientist , Small Molecule Analytical Research & Development** The Small Molecule Analytical Research and Development (SMAR&D) ... group has an exciting opportunity for a Principal Scientist based in Rahway, NJ. Join...sterile and combination products. You will also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities… more
- Merck (Rahway, NJ)
- …of our company's Research Laboratories Division is seeking applicants for a Principal Scientist position available at our company's research facility. The ... Principal Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists… more
- ThermoFisher Scientific (New Brunswick, NJ)
- …and Drug Products across internal and external manufacturing sites. The principal scientist reports to the Associate Director of GBS and is responsible for ... stability protocols, and preparation, review and approval of CMC elements of regulatory filings to support the activities of the Global Biologics Stability program… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- City of New York (New York, NY)
- …compliance, and capital projects engineering and construction review and approval. Provide principal regulatory oversight and sanitary survey for the NYC ... including program management, resource allocation. Key program activities include regulatory inspections, issuance of commissioner's orders, bathing establishments engineering… more
- Bristol Myers Squibb (Madison, NJ)
- …acting on Clinical Trial data to support development, and + Serving as principal functional author for Regulatory submission, study reports, and publications + ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Director , Early Clinical Development (MD) - Hematology & Cell Therapy with Focus… more
- Bristol Myers Squibb (Madison, NJ)
- …and acting on clinical trial data to support development + Serving as principal functional author for Regulatory submission, study reports, and publications + ... their personal lives. Read more: careers.bms.com/working-with-us . **Job Title** Director , Early Clinical Development - Immunology **Functional Area Description**… more
- Merck (Rahway, NJ)
- …Summary** + Under the guidance of a senior leader, an Associate Principal Scientist /Associate Director , has primary responsibility for planning/managing ... barriers to reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategy and programs + In… more