- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director (Distinguished Scientist ) has primary responsibility for the planning and directing of clinical research activities ... and will interact externally with key opinion leaders.-Specifically, the Executive Director may be responsible for:Evaluating pre- clinical and translational work… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …manufacturing organizations CMO. This position serves as the Regulatory Affairs (RA) CMC project representative to the CMC sub team and the RA team and serves ... as ad hoc member to the Global Project Team for late stage projects. This position manages...technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing… more
- Merck & Co. (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 us and experience...You will also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities will include:-Driving our company's… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire… more
- United Therapeutics (Research Triangle Park, NC)
- …is not currently an option. **Who you are** We are seeking a highly motivated Clinical Drug Development Scientist to join our team. You will support the design, ... protocols and general proficiency with drug development strategy. The Clinical Drug Development Scientist will assist with... clinical development with a PhD/PharmD + For Clinical Drug Development Associate Director level: +… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Sr. Director / Executive Director - Safety Data Scientist ** **Purpose:** The purpose of the Sr. Director ... / Executive Director - Safety Data Scientist role is to provide strategic leadership for the technology, systems, automation, and analytics strategy across… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Provides medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams. **Responsibilities** + Study Strategy: ... size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member...oversee completion of clinical trial protocols.… more
- BeOne Medicines (Emeryville, CA)
- General Description: _The Director , Safety Scientist supports assigned compounds in conjunction with Product Safety Leads (PSLs) and leverages clinical and ... may have direct reports depending on the program / portfolio being led. The Director , Safety Scientist provides key support as an experienced safety scientist… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Distinguished Scientist , Safety Assessment Project Expert **Location** : Cambridge, MA Morristown, NJ **About the Job** Are you ready to shape the ... providing toxicology and safety pharmacology expertise as a member of global project teams. Given the activities performed by the group, internal (within Preclinical… more
- Takeda Pharmaceuticals (Boston, MA)
- …you and empower you to shine? Join us as a PV Risk Management Scientist /Associate Director . At Takeda, we are transforming the pharmaceutical industry through ... for excellence in everything we do. As an Associate Director / PV Risk Management Scientist , being part...assessment document + Engages with partner global functions (eg Clinical Science, Med Affairs, Regulatory Affairs, Biostats) to ensure… more
- Bristol Myers Squibb (Cambridge, MA)
- …facilitates the transition of drug candidates from early to late-stage clinical development, their approval and life cycle management. Early-stage translational ... the development, and maximize the potential, of BMS's therapies post- clinical proof-of-concept, including registrations and life-cycle management. Translational disease… more
- Veterans Affairs, Veterans Health Administration (Fayetteville, NC)
- Summary The Supervisor serves as a Supervisory Clinical Laboratory Scientist for the Pathology and Laboratory Medicine Service (P&LMS) at the Fayetteville VA ... Laboratory Director ) for managing and supervising all phases of clinical laboratory service operations. Responsibilities 1. The Laboratory Manager provides first… more
- University of Florida (Lake County, FL)
- Data Scientist IV - UF Clinical and...IV position. This position will work with the PHRC Director as part of the leadership team to develop, ... Administration/Support Department: 29680302 - MD-CTSI-VILLAGES HEALTH CRC Classification Title: Data Scientist IV Job Description: The UF Health - Precision Health… more
- Lilly (Indianapolis, IN)
- …the application of scientific and medical training, clinical expertise, and relevant clinical experience, the Clinical Research Scientist - Clinical ... various medical activities in support of demand realization. The Clinical Research Scientist must be aware of...submissions (eg, annual reports) according to the agreed upon project timeline. + Provide protocol oversight and input into… more
- AbbVie (North Chicago, IL)
- …. Job Description Purpose: The Senior Principal Research Scientist / Director of Drug Metabolism and Disposition (Biotransformation) ... in designing and executing biotransformation studies, including both nonclinical and clinical studies. + Develop and implement strategic plans for drug metabolism… more
- Merck (Rahway, NJ)
- **Job Description** **The Executive Director (Distinguished Scientist ) has primary responsibility for the planning and directing of clinical research ... and will interact externally with key opinion leaders. **Specifically, the Executive Director may be responsible for:** + Evaluating pre- clinical and… more
- Unilever (Hoboken, NJ)
- …and lead as well as follow and support others. JOB RESPONSIBILITIES: The Nutrition Clinical Scientist will play a critical role in the Nutritional Sciences and ... clinical research to underpin the science behind product claims. The Nutrition Clinical Scientist will provide subject matter expertise in clinical … more
- Merck (Bismarck, ND)
- **Job Description** **Role Summary:** + The Global Director Medical Affairs (GDMA) is responsible for supporting the execution of scientific & medical affairs plans ... regions. + Serves as an impactful member of Product Development Team sub-teams (eg, Clinical , V & I, Commercial, Publications). + Contributes to the development of a… more
- Bristol Myers Squibb (Madison, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . The Early Development Clinical Scientist function provides scientific expertise necessary to ... Submit clinical documents to TMF. **Reporting Relationship** + Report to Director , Clinical Scientists, Early Development or higher **Degree Requirements** +… more
- Lilly (Indianapolis, IN)
- …and development of new medicines from preclinical lead molecule identification to clinical post-drug approval, with the goal of identifying and developing the right ... in this subject area, we are seeking a scientific director who will lead a group of quantitative systems...allocation and staff development. + Provide scientific leadership to project teams to support the selection of the right… more
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