- Merck & Co. (Rahway, NJ)
- …of regulatory submissions. -Under the general scientific and administrative direction of Associate Principal Scientist , and working in conjunction with internal ... and external partners, this person will support mid-late stage and commercial cell bank-related projects for large molecule programs. The person will be responsible for commercialization activities on late-stage pipeline and/ or post-market commercial… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for Development : Manages multiple CMC development projects. Leads submission teams with supervision. Acts as point of contact to cross-functional teams on US/EU RA ... Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging… more
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist / Associate Director, has primary responsibility for ... planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally.Types of studies executed include… more
- Merck & Co. (Rahway, NJ)
- Job Description Senior Principal Scientist , Precision Medicine, Immunology Precision Medicine is an integral part of our Immunology Therapeutic Area. To support ... reviewing concepts aligned with the Precision Medicine goals for relevant programs/assetsThe Senior Principal Scientist is responsible for maintaining a strong… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Senior Director ( Sr . Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving ... span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …potential? The Position This position has the responsibility of working with senior level Scientists and technicians to execute process development, scale-up, tech ... Flexibility in schedule is required for this role. Relationships Reports to: Lead Scientist (Supervisor) Essential Functions May perform one or more of the following… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Executive Director (Distinguished Scientist ) has primary responsibility for the planning and directing of clinical research activities involving ... business development assessments of external opportunities.Managing other Directors and/or Senior Directors responsible for Atherosclerosis clinical development projectsThe Executive… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …tomorrows. **Job Description** Attribute Sciences is seeking a talented and highly motivated Senior Associate Scientist with a background in immunology, cell ... to assess the functional phenotype of immune cells. The Sr . Associate Scientist will perform...day-to-day work. We are creating Kite together, with the recognition that the best teams are built by the… more
- Cambrex High Point (Waltham, MA)
- …be the first to be notified when suitable Associate Scientist and Senior Associate Scientist opportunities arise within our Chem istry Department at ... seeking exceptional candidates for its Associate Scientist or Senior Associate Scientist position in Waltham, MA. A successful candidate will be… more
- Catalent Pharma Solutions (Kansas City, MO)
- **Quality Control Associate Scientist ** **Position Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose ... in Kansas City, MO is hiring a Quality Control Associate Scientist . The Quality Control Associate...plan / schedule developed with input from supervisor or senior team member + Maintain high quality documentation in… more
