- Merck & Co. (Rahway, NJ)
- …the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to clinical ... of the strategic elements of drug development. As a subject matter expert, the Director within the QP2-IO Group will work closely with teams of highly collaborative,… more
- Merck & Co. (Rahway, NJ)
- …Point, PA / Rahway, NJ is seeking a curious and collaborative Director to support our rapidly expanding cardiology respiratory, metabolism and ophthalmology ... pipeline.As a Director , you will serve as an expert QP2 representative...teams of experienced scientists to discover and advance the clinical development of novel therapeutic agents for cardiac, respiratory,… more
- Merck & Co. (Rahway, NJ)
- …of clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direcUindirect team members ... drives scientific planning, strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead,...under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving ... in Immunology. With a focus on late-stage development, the Clinical Director will manage the entire cycle...under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in… more
- Tris Pharma (Monmouth Junction, NJ)
- …an immediate opening for a full-time permanent Director /Senior Director , Clinical Quality Assurance. This is a hybrid position. Job Title commensurate ... with experience.SUMMARY:Reporting to the Chief Quality Officer the Senior Director of Clinical Quality Assurance provides strategic leadership and direction for … more
- Merck & Co. (North Wales, PA)
- Job DescriptionReports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the ... promotional messages and claims (aligned with marketing strategy) in clinical trial design and product labeling as it relates...under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in… more
- Merck & Co. (Rahway, NJ)
- …GCTO organization prepares a variety of regulated documentation in support of the clinical development portfolio and compliance in public disclosure of clinical ... results, document disclosure, and data sharing with external researchers. The Executive Director in Medical Writing will be responsible for overseeing clinical … more
- Merck & Co. (Rahway, NJ)
- …(GPL) is responsible for overseeing and managing Global Regulatory Affairs & Clinical Safety (GRACS) global business processes. This includes defining and optimizing ... under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in...office-based positions in the US will be working a Hybrid work consisting of three total days on-site per… more
- Merck & Co. (Rahway, NJ)
- …role of Associate Director . The team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... clinical pharmacology and pharmacometrics of oncology drugs from post-PCC...communication skills. As a subject matter expert, the Associate Director within the Group will work closely with teams… more
- Merck & Co. (Rahway, NJ)
- …provides a high degree of technical and project management responsibility. The Associate Director - Process/Facility Lead position will report to the Director , ... Responsibilities include the following:The process/facility lead role at the Associate Director level will serve as a technical mentor and operations team… more
- Merck & Co. (North Wales, PA)
- …with talented and dedicated colleagues while developing and expanding your career.The Clinical Director (Principal Scientist) has primary responsibility for the ... medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage...under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in… more
- Merck & Co. (Rahway, NJ)
- …launch pad for the early phase and commercial formulation development and GMP clinical supply manufacture of our Company's drug product pipeline.- The FLEx Process ... will be required to ensure effective process development in support of clinical development.- -The Process Engineering Lead stands at the vanguard of commercial… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are currently recruiting for an Associate Director Global Oncology Marketing Hematology for a non-covalent inhibitor in Leukemia and Lymphoma.- A ... to help patients and expand our company's oncology hematology portfolio.The Associate Director of Global Oncology Marketing will report to the Hematology Asset &… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Executive Director , Global Medical and Scientific Affairs (EDMA) GYN Malignancies is accountable for the development and execution of scientific & ... medical Value and Implementation (V&I) plan, in collaboration with the Executive Director of Scientific Affairs (EDSA), that guides TA scientific exchange (input and… more
- Merck & Co. (Rahway, NJ)
- …approach, driving the development of in vitro-in vivo relationships and preclinical-to- clinical translation in bioperformance of formulationsThe Director will ... oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Director , Global Market Access, Immunology T he Director , Global Market Access, Immunology will play a leadership role in ... strategy for assets within our Immunology portfolio. In this role, the Director will lead the development and execution of global market access strategy,… more
- Merck & Co. (Rahway, NJ)
- …Pharmaceutical Administration, Public Health, Health Policy, Medicine, or Clinical Pharmacy)5+ years relevant experience following advanced or professional ... under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in...office-based positions in the US will be working a Hybrid work consisting of three total days on-site per… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Global Director Medical Affairs (GDMA) Oncology Assets & Pipeline coordinates the development and implementation of the Global Medical Affairs ... goals and strategies that inform and demonstrate scientific & clinical value and address insights from affiliates and regions...under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5, 2023, employees in… more
- Merck & Co. (Rahway, NJ)
- …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions,… more
- Merck & Co. (Rahway, NJ)
- …Our company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle ... placement, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director may be responsible for:Evaluating pre- clinical and… more
