- Merck & Co. (North Wales, PA)
- Job DescriptionPosition Responsibilities The Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert ... the comprehension of scientific foundations and goals for approved, in- development , and active Company-sponsored trials and/or investigator-sponsored research studies.… more
- Merck & Co. (Rahway, NJ)
- …Business Operations Lead is expected to understand the end-to-end regulatory submission process . The main focus will be on document production processes, including ... management solution and function as BSOLead the Change Management and Business Process activities to drive adoption of the new solutionSupport daily operations of… more
- Insmed Incorporated (NJ)
- …and for the future of science, we're in. Are you?About the Role:The Director of Clinical Supply Chain Operations is responsible for leading global demand planning ... plans for production, packaging, distribution, and clinical supply budgeting. The Director provides strategic leadership for Clinical Supply Chain & Logistics… more
- Merck & Co. (Rahway, NJ)
- …highly experienced and motivated individual to join our team as the Director of Biologics- Materials and Biophysical Characterization. The successful candidate will ... plans for biophysical characterization to support the research and development of biopharmaceuticals.Oversee the design, execution, and interpretation of experiments… more
- Merck & Co. (South San Francisco, CA)
- …California, Colorado and other US State Acts - Required Skills: Business Development , Communication, Drug Discovery Process , High Performance Team Building, ... Job DescriptionThe Executive Director of Metabolism & Obesity will be responsible...to collaborating with key opinion leaders in academia.Lead the development and implementation of in vitro and in vivo… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …ensure harmonization, alignment and execution of regulatory guidelines across all manufacturing areas, supporting both clinical and commercial sites. This individual ... to ensure harmonization and alignment across all functions and sites.Support the development of the GMP Compliance program related to clinical/ commercial stage and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and retain all the records in order to ensure the traceability of audit process . Participate in the development of GMP audit certification program to ensure ... lessons learned from audits, assessments, inspections, metrics, deviations and or process improvements. Ensure adequate QA oversight of the GMP audit programs… more
- Merck & Co. (Rahway, NJ)
- …are currently seeking a Cardiovascular & Respiratory Competitive Intelligence Director specializing in PAH, COPD, and other cardiopulmonary diseases. This ... benchmarking, and recommendations for commercialization strategies, portfolio prioritization, clinical development /research strategies, and Business Development initiatives.Partnering with… more
- Merck & Co. (Boston, MA)
- …and other stakeholders. The scope of this group includes strategy development , strategy execution and value realization, enterprise strategic planning, risk ... establish capabilities needed for our Company's Oncology Research & Development to be successful.This individual will collaborate cross-functionally with Oncology… more
- Merck & Co. (MA)
- …commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring ... activities involving investigational compounds in Immunology. With a focus on late-stage development , the Senior Clinical Director will manage the entire cycle… more
