- 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)
- …Description** **Role Summary** + Under the guidance of a senior leader, a Principal Scientist / Director , has primary responsibility for developing value ... to reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs + In… 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
- New York University (New York, NY)
- …In this role, the Project Coordinator will work closely with the Lead Principal Investigator (CVR Co-Executive Director and Chief Research Officer), Project ... protocols) and ensure accessibility via shared platforms. * Assist the Lead Principal Investigator and Project Director in tracking budgets and expenses… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- We are looking for a highly motivated Principal Scientist , Clinical Pharmacology in our Pharmacometrics (PMx) group. The position will report to the Senior Group ... Director (SGD) within Clinical Pharmacology (CP.) You will represent...into clinical study reports + Provide CP support of regulatory documents, communications, and presentations (eg, IND, health authority… 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