- Teva Pharmaceuticals (Parsippany, NJ)
- Director , Therapy Area Head, Global Regulatory Medical Writing Date: Aug 22, 2024 Location: Parsippany, United States, New Jersey, 07005 Company: Teva ... candidate can sit anywhere in the United States** A Director , in Global Regulatory Medical Writing , reports into Head of Global Regulatory Medical… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …research areas centered around rare diseases and immune disorders. **Job Summary:** The Associate Director of Regulatory Writing is a key role responsible ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...strategic insights at the study team level. The Associate Director of Regulatory Writing must… more
- Intra-Cellular Therapies, Inc (Bedminster, NJ)
- …of bipolar depression in adults as monotherapy and as adjunctive therapy. The Associate Director / Director of Medical Writing provides support for the ... Regulatory documents, and responses to health authority information requests. The Associate Director / Director of Medical Writing must have experience… more
- Merck (Rahway, NJ)
- …diagnostic regulations on the development and registration activities for the respective medical products. + Providing regulatory support for due diligence ... **Job Description** Our Diagnostics focused Regulatory Affairs team helps bring new precision medicine advancements to the world by facilitating effective,… more
- Bristol Myers Squibb (Madison, NJ)
- …external resources; ensure appropriate quality controls in place for compliant submissions + Writing regulatory documents (eg new INDs, briefing book content, BT ... careers.bms.com/working-with-us . **Position Responsibilities** + Develop global and/or US regulatory strategy for Oncology products in development and through life… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …real-world evidence, and creating hope for all facing illness. As a senior member of Medical Science, the Senior Director , Medical Science - Early Stage will ... therapeutic areas involving complex indications including rare disease/orphan conditions. The Senior Director , Medical Science - Early Stage will be responsible… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …and experienced individual to join the **PS Strategic Operations** team as a ** Director , PS Medical Device Safety** responsible for developing and leading ... drive strategies and ensure operational excellence through successful business partner collaboration. The Director , PS Medical Device Safety will be a medical… more
- Merck (Rahway, NJ)
- …, Operations, Non-clinical, Clinical, and other functional areas + Experience with regulatory submissions including writing / review of regulatory ... robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …interpreting clinical results and provide a guidance to prepare high quality reports working with Medical Writing + Working with Medical Writing team, ... documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Director , Clinical Development will provide… more
- HSS (New York, NY)
- …our Mission, you too can be part of our transformation across the enterprise. Director of Nursing Quality and Magnet Program Full-Time On site Overview: The ... Director of Nursing Quality and Magnet Program is responsible...oversight of nursing quality improvement initiatives, ensuring compliance with regulatory and accreditation standards, and leading the Magnet Recognition… more
- J&J Family of Companies (Raritan, NJ)
- …Global Development (clinical trial startup, performance, oversight, and results reporting), Medical Writing (document templates and clean authoring), Therapeutic ... At least 10 years' of relevant pharmaceutical/scientific experience (in clinical development or medical writing preferably) + At least 10 years' of people… more
- Research Foundation CUNY (New York, NY)
- Job Title: Director of Grants & Sponsored Programs PVN ID:...City College of New York (CCNY), is the only medical school in the City University of New York ... Studies (PA). Our mission is to provide access to medical education to talented individuals from social, ethnic and...Reporting to the Associate Dean for Research, the GSP Director manages and supports full-time staff and works closely… more
- HSS (New York, NY)
- …too can be part of our transformation across the enterprise Clinical Services Director (RN) Full-Time Position Summary: The Clinical Services Director is ... delivery, improving operational efficiency, and ensuring compliance with hospital and regulatory policies and practices at HSS ambulatory locations. Drawing on a… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …respected - is a research-driven pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. MTPC has discovered and produced several ... treatments for difficult-to-treat diseases and commercializing products with significant unmet medical needs in North American markets. In the United States, MTPA… more
- Pfizer (New York, NY)
- …teams to follow and ensure more complete evidence packages are available to support regulatory , launch, and post-launch strategy. The IEP Director is a member of ... the respective RWE Leads for the asset. The IEP Director draws from robust knowledge of the drug development...colleagues involved in the IEP process (CMAOs, CSI, Clinical, Regulatory , Safety, GAV, Patient Advocacy, and others) + Contribute… more
- Bristol Myers Squibb (Madison, NJ)
- …members. **Key Responsibilities** + Develops expertise beyond biostatistics by researching the medical literature, regulatory and HTA documents to develop an ... careers.bms.com/working-with-us . **Position Summary** The Market Access/HEOR GBDS Associate Director provide statistical support to Market Access/HEOR activities. In… more
- NJ Transit (Newark, NJ)
- …contracts and associated change through the life cycle of the contract. + The Director must understand the regulatory and statutory basis for all procurements ... Director Procurement Procurement & Support Services Job Description:...Relationship Management . + Must be proficient in Contract Writing and Negotiations. + Must understand the regulatory… more
- AbbVie (Madison, NJ)
- … filings and anticipates regulatory questions. Leads CLINICAL PHARMACOLOGY regulatory documents writing , submission and response to Regulatory ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Facebook, Instagram, YouTube and LinkedIn. Job Description As a Director within the Clinical Pharmacology Neuroscience Group at AbbVie,… more
- AbbVie (Florham Park, NJ)
- … filings and anticipates regulatory questions. Leads CLINICAL PHARMACOLOGY regulatory documents writing , submission and response to Regulatory ... medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's… more
- J&J Family of Companies (Raritan, NJ)
- …experience. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance) including at ... Associate Director , RA Labeling Product Leader (1 of 2) -...least 6 years of direct regulatory labeling content experience developing and writing labeling… more