- Daiichi Sankyo, Inc. (Bernards, NJ)
- …This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product ... more
- Merck & Co. (Rahway, NJ)
- …development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an experienced ... more
- Merck & Co. (Rahway, NJ)
- …sites, manufacturing investigations, process validation, and authoring of regulatory submissions. -Under the general scientific and administrative direction ... more
- Merck & Co. (Rahway, NJ)
- …as a lead GCS Planning program representative ) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines ,- strategies ... more
- Merck & Co. (Rahway, NJ)
- …products. Our team is looking for a candidate for the position of Associate Principal Scientist (R4) focused on developing parenteral drug products across a range ... more
- Merck & Co. (Rahway, NJ)
- …Analytical Research and Development (SMAR&D) group has an exciting opportunity for an Associate Principal Scientist based in Rahway, NJ. Join us and experience our ... more
- Merck & Co. (Rahway, NJ)
- …areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of ... more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP) will be responsible for leading the Translational Medicine (TMed) Cardiovascular & Respiratory Therapeutic Area and ... more
- Merck & Co. (Rahway, NJ)
- …Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical Development ... more
- Merck & Co. (Rahway, NJ)
- …(eg GxP) Understanding of pharmacovigilance-related IT systems, data and gateways/interfaces with regulatory bodies such as the EMA and FDA Proven ability to bridge ... more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small molecules ... more
- Merck & Co. (Rahway, NJ)
- …contributions and scientific supervision of a biochemical team, the Associate Principal Scientist collaborates with cross-functional teams to deliver manufacturing ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. JOB SUMMARYThe Associate Director, GMP QA Process Excellence is accountable to collect information, ... more
- Merck & Co. (Rahway, NJ)
- …reimbursement and market access, and provide input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs.In ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …well as FDA regulation requirements, industry best practices and will withstand regulatory inspections by regulatory authorities and regular audits.Drug Product ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diseases and immune disorders. SummaryReporting to the Senior Director, I&A, the Associate Director, Global Oncology Forecasting will drive creation of demand and ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …ensure consistency and compliance in case processing and adherence to regulatory guidelines.Qualifications: Successful candidates will be able to meet the ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.- CRO / Vendor ... more
