- Merck (Trenton, 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 (Upper Gwynedd, PA)
- **Job Description** In this Sr. Principal Scientist / Director position within Translational Oncology, this team member will provide leadership for aligned and ... Teams (ADTs) and our diagnostic partners. Position reports to Executive Director , CDx. **Primary Responsibilities** : + Direct CDx/IVD development projects,… more
- Merck (Upper Gwynedd, PA)
- …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
- Bristol Myers Squibb (Princeton, NJ)
- …oncology. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external ... human genetics, immunology). + Minimum of 6 years post-PhD experience for Sr. Principal Level (and minimum of 8 years Post-PhD experience for AD Level), with… more
- Merck (North Wales, PA)
- **Job Description** The Senior Director (Senior Principal Scientist ) has primary responsibility for the planning and directing clinical research activities ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Senior Director … 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
- 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 (Princeton, 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 (Princeton, 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 (North Wales, PA)
- …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