- Merck & Co. (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …you ready to maximize your potential with us? The Position As the Associate Director of Strategic Market Insights, the functional responsibilities include ... industries, and other external issues as directed and set by Sr. Director , Enterprise Market Intelligence ; enhancing company marketplace position by leveraging… more
- Merck & Co. (Millsboro, DE)
- Job DescriptionOur company seeks to add an Associate Director . Veterinarian Services at our Millsboro, Delaware location. This position will have overall ... (USDA, DEA, DNREC, etc.) of animal facilities and program reviews is required.PurposeThis Associate Director will report to the Site Quality Head/ Director … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Scientist, Device Risk Management Lead, is a crucial member of our team, responsible for spearheading risk management efforts ... through launch and post-market surveillance. Key Responsibilities and Activities: The Associate Principal Scientist, Device System - Device Risk Management will be… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryReporting to the Senior Director , I&A, the Associate Director , Global Oncology Forecasting ... will drive creation of demand and revenue forecasts. The Associate Director is a dynamic member of the Global Oncology I&A Team and partners closely with Market… 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 Nordisk is one...internal stakeholders. In the execution of specific projects, the Associate Director , will be accountable for managing… 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 ... formulation, manufacturing process, and primary packaging to enable phase appropriate regulatory filings for large molecule sterile products. -These sterile products… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Extensive experience in project management, process, product, and/or analytical development activities and pharmaceutical/oncology project development preferred- 1 ... or More Years Extensive knowledge of global CMC regulatory requirement and preferably NDA or BLA/MAA submission experiences for oncology area preferred TravelAbility… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Associate Technical Lead as part of the Technical Operations team based in ... Raritan, NJ. Role OverviewThe Associate Technical Lead will be part of Technical Operations...Responsibilities This individual with provide direct support to the Director of Manufacturing Excellence by providing technical expertise to… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …optimization of organizational resource allocation. Relationships Reports into CDO Operations Director / Associate Director . Establish and manage relationships ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...overall business objectives. Align on project strategy with Portfolio Director and TA heads Solutions Oriented: Proven ability to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …integrity, and timelines for assigned studies and escalates issues to the Associate Director of Medical Coding to gain resolution. Functional Expertise:Study ... conventions. Reviews and submits DS Medical Coding synonym list update requests to the Associate Director of Medical Coding to ensure accuracy and consistency of… more
- Merck & Co. (Rahway, NJ)
- …that delivers high quality data and clinical supplies. This position reports to the Associate Director of Global Clinical Supplies Quality and is critical to ... the rights and well-being of patients; comply with applicable global regulatory requirements through sound processes and procedures, and to provide independent… more
- Merck & Co. (Rahway, NJ)
- …Infrastructure Engineering - Migration Services Solution EngineerUnder the direction of Associate Director , Technical Product Management, Migration Services, the ... in development of complex initiatives supporting enterprise programs.Problem-solving and analytical skills: Proven ability to analyze complex technical issues and… more
- Fidelity Investments (Boston, MA)
- …business development, product, fund operations, and business operations.The RoleAs a compliance associate for the digital asset team, you will build and maintain ... monitor the design and operating effectiveness of controls; track legal and regulatory changes and trends; identify and resolve digital assets compliance issues; and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …their aspirations. Join Gilead and help create possible, together. **Job Description** ** Associate Director , Analytical Regulatory Sciences, Systems ... is a site based position located in Foster City, CA_** The Associate Director , Analytical Regulatory Science, collaborates with product development,… more
- Merck (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …virus (AAV), siRNA, and other biologics. **A Typical Day in the Role of Associate Director Might Look Like:** + Lead the development of LC-MS/MS assays ... skilled and motivated leader in bioanalytical and biomarker analysis to join the Analytical Chemistry Group, located in Tarrytown, NY. In this role, you will lead… more
- Gilead Sciences, Inc. (Foster City, CA)
- …regulatory strategies for assigned products or projects. + Demonstrates advanced regulatory and business knowledge and advanced analytical abilities, as ... their aspirations. Join Gilead and help create possible, together. **Job Description** Regulatory Advertising and Promotion (RA Ad/Promo) is a core function within… more
- Mount Sinai Health System (New York, NY)
- **Job Description** The Assistant Director will oversee the regulatory component of the human research protection program at Mount Sinai. Responsible for all ... regulatory knowledge relating to human research, including federal, state,...SOPs/forms/worksheets/checklists. + **Program Quality Analysis and Improvement** + Perform analytical and evaluative work associated with program activities; develop… more
- Otsuka America Pharmaceutical Inc. (Rockville, MD)
- **Job Summary** Associate Director , Quality Control, Biologics is responsible for late development stage through commercial biologic products including product ... productive collaborations with internal QA, Quality Control, Clinical Development, and Regulatory teams. **Job Description** + Manage analytical method… more
