- Novo Nordisk Inc. (Plainsboro, NJ)
- …to providing medical education and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps us all marching to the ... the head of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …drug and device safety reporting regulations. Relationships Reports to Patient Safety Management . Daily internal interactions with personnel from Patient ... to providing medical education and collecting data to support efficacy and new product development , CMR is involved. The one thing that keeps us all marching to the… more
- Merck & Co. (Rahway, NJ)
- …who is passionate about lab management and operation support. The Associate Director of Biologics Process Research and Development (BPR&D) is responsible ... (PM/CM). The US Associate Director is also responsible for leading lab safety and equipment training for new hires, as well as maintaining daily lab 5S… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(CSPs) and Informed Consent Forms (ICFs), for assigned product(s)Authors or oversees the development of the Safety Management Plan for assigned ... and communicates issues, as appropriate. Oversees or leads the coordination of Safety Management Team (SMT)/Product-level safety meetings, maintains roster,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Method Development & Testing is responsible for leading a Center of Excellence (CoE) focused on developing and ... across development to commercialization.Collaborate with Analytical Research & Development (AR&D), Design Controls & Risk Management (DCRM), Quality,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Principal Statistical Programmer - Oncology (Hybrid) In BARDS (Biostatistics and Research Decision Sciences), a ... distinguished department within our Company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director of Quality Project Management and Strategyas part of the ... Quality team based in Raritan, NJ. Role OverviewThe Associate Director of Quality Project Management and Strategy role is an exempt level position with… more
- Merck & Co. (North Wales, PA)
- … Associate Principal Scientist, Statistical Programmer supports the design, development , and delivery of efficient, flexible, and modular analysis and reporting ... a distinguished department within our Company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter… more
- Tris Pharma (Monmouth Junction, NJ)
- …Junction, NJ headquarters has an immediate need for an experienced Associate Director/Director, Analytical Research & Development . Job Title commensurate ... with experience.SummaryThe Associate Director/Director, Analytical Research and Development (R&D) leads Analytical Research and Development (AR&D) teams in… more
- Merck & Co. (North Wales, PA)
- … Development projects (data, analyses, tables, graphics, listings)Strong project management skills; leadership at a program level; determines approach and ensures ... submissionsEnsure programmatic traceability from data source to modeling resultSupport the development of programming standards to enable efficient and high quality… more
- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... DNREC, etc.) of animal facilities and program reviews is required.PurposeThe Associate Director/Attending Veterinarian will report to the Site Quality Head/Director… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … development of commercial strategies Excellent writing, presentation, project management and strong influencing skills required. Solid communication skills with ... formulating business relevant strategic recommendations Strong understanding of drug development , commercialization, and lifecycle management Works independently… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Clinical Operations, Clinical Development , Biostatistics and Data Management , Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical Safety ... areas centered around rare diseases and immune disorders.Job Summary Deliver the development and implementation of informatics systems and programs to support the… more
- Merck & Co. (North Wales, PA)
- …of statistical datasets that support multiple stakeholder groups which include clinical development , outcomes research and safety evaluation.The position is a ... Sciences), a distinguished department within our renowned Research and Development division, quantitative scientists, in partnership with other subject matter… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …in reviewing proposals and selecting vendors. This position also supports the management of the WO development and implementation.Supports packaging design and ... projects and/or identification of issues which may compromise patient dosing or safety . Basic understanding of professional working environment as well as Quality… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking an Operations Associate as part of the Technical Operations team based in Raritan, NJ.Role ... complete production tasks required by shift schedule.Aid in the development of manufacturing processes including appropriate documentation.Drive continuous improvement… more
- Merck & Co. (South San Francisco, CA)
- …Modeling, Data Science, Data Visualization, Machine Learning, Software Development , Stakeholder Relationship Management , Waterfall Project ManagementPreferred ... Job DescriptionThe Computational Toxicology group within the Nonclinical Drug Safety (NDS) division at our company is actively seeking an enthusiastic AI/ML data… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …3rd party development . This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS) ... may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU....through all labeling discussions with the FDA/CHMP while ensuring management alignment. Strategizes and plans for FDA meetings as… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for development products (if applicable) Provide input to preparation of Development Safety Update Reports (DSURs), periodic SUSAR reports, Periodic ... safety surveillance sub-function within the US East Coast Development Hub comprised of Senior Global Safety ...include Healthcare professionals, HAs, ECs, DMCs, and Academia. Line management of Senior Global Safety Lead(s), Global… more
- Merck & Co. (Rahway, NJ)
- …mentor talentStrategic and critical thinking to advance sterile product development strategyProject management skillsAttention to technical detailBuilds ... through past scientific / technical expertise).Experience in budget planning & management , establishing development strategies, and managing scientific staff… more
