- Genmab (NJ)
- …biological, pharmaceutical science or related discipline Minimum of 8 years of experience in clinical research with at least 4 or more years of drug development ... (including clinical trial implementation, and oversight of all aspects of clinical development) working closely with the Medical Director and other… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionTitle: Associate Principal Scientist/ Associate Director , Outcomes ResearchRole SummaryUnder the guidance of a senior leader, an Associate ... resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses,… more
- Merck & Co. (Rahway, NJ)
- … research organizations, database holders, and others.To prepare outcomes research protocols, statistical analysis plans, and clinical study reports.To ... to inform healthcare decision making.- This position will provide global outcomes research support for the Oncology programs.- The position reports to the Senior… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. Summary This position works with the Director , Clinical Study Startup to establish the strategy driving global ... make decisions where appropriate and escalate any complex problems to the Director , Clinical Study Startup.This position requires strong organization and… more
- Merck & Co. (Rahway, NJ)
- … Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the guidance of a supervisor, the Director has ... primary responsibility for the planning and directing of clinical research activities involving new or marketed...medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage… more
- Genmab (NJ)
- …to the effective planning, and timely delivery of complete, high quality and reliable clinical trial data. The Associate Director DM will provide oversight ... be our best, and authentic is essential to fulfilling our purpose.The Role:An Associate Director , Data Management is operationally responsible for the oversight… more
- Merck & Co. (Rahway, NJ)
- …Clinical Supply organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full company Research Laboratories ... portfolio of clinical trials.- Global Clinical Supply is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary Oversees typically ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery of a ... single or multiple clinical trials from strategy outline through to CSR by...has invented next-generation antibody technology platforms and leveraged translational research and data sciences, which has resulted in a… more
- Merck & Co. (Rahway, NJ)
- …manufacturing to manage clinical development projectsAssist the Senior Director , Associate Vice-President/Vice-President and Product Development Team Lead in ... Job DescriptionThe Clinical Director (Principal Scientist) has primary...has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in… more
- Merck & Co. (Rahway, NJ)
- … Clinical Development, has primary responsibility for the planning and directing clinical research activities involving new or marketed drugs in the Oncology ... Clinical Research group and in the field...will interact externally with key opinion leaders.-Specifically, the Executive Director , PDT lead may be responsible for:-Evaluating pre- clinical… more
- Merck & Co. (Rahway, NJ)
- …the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with teams… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate ... on a continuous basis in decision making and driving pipeline impact. The Associate Director will perform job duties independently with minimal supervision… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … research areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for ... producing scientifically accurate, high-quality clinical regulatory documents while adhering to regulatory guidelines. This...and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …the head of Clinical , medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small ... small molecules, biologics, and vaccinesBroad understanding of drug discovery, development and research , clinical data coding and experience working within a… more
- Merck & Co. (Rahway, NJ)
- …oversight of, contractors performing various GMP activities supporting the production of clinical supplies with focus on API. The position will be heavily involved ... diverse pipeline Serving as the bridge for quality oversight between research and development and commercialization activities. Communicating, and serving as Quality… more
- Genmab (Plainsboro, NJ)
- …authentic is essential to fulfilling our purpose.The RoleGenmab is looking for an Associate Director , Global Regulatory Affairs, Regulatory Strategy to be a part ... US RA in the Global Regulatory Team, Labeling Working Groups, Launch Teams, Clinical Trial Teams, and other cross-functional teams as required for the assigned… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders. Summary Position leads ... Authorities globally with some supervision. This position also guides contract research organization (CRO) programmers and statisticians in preparing analysis files… more
- Merck & Co. (Rahway, NJ)
- …risk management techniques to positively support and influence clinical and commercial combination product development and launches.Principal ResponsibilitiesLead ... to ensure full integration of the device development activities with the clinical , regulatory, formulation, commercial and other key of our company's functions.Lead… more
