- Merck (West Point, PA)
- **Job Description** The Global Clinical Supply (GCS) organization is within our company's Research Laboratories and is accountable for managing the 'end-to-end' ... the business for the design, assessment, and improvement of the end-to-end processes. The Associate Director , GCS Process Steward, is accountable to assure that … more
- Bristol Myers Squibb (Princeton, NJ)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , Clinical Data Standards is a leadership role ... This role reports to Director or Executive Director , Head Standards Management & Steward within Clinical...preferred **Experience Requirements** + At least 12 years of global clinical trial expertise and a successful… more
- Merck (North Wales, PA)
- …our company, a premier research-intensive biopharmaceutical company. We are seeking an Associate Director , Clinical Systems Implementation to manage ... to the successful implementation and use of multiple applications. + Represent Global Clinical Trial Operations (GCTO) (business) in application related… more
- Bristol Myers Squibb (Princeton, NJ)
- …**Position Summary:** We are seeking a highly motivated and detail-oriented Associate Director - Product Manager with broad clinical data experience to join ... to drive cross-functional collaboration. The Product Manager will work closely with global clinical , biometrics and data science stakeholders, including data… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... obtain labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling Oversight Committee - GLOC) driving cross-functional collaboration and… more
- Bristol Myers Squibb (Princeton, NJ)
- …, this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to build and ... integrate one global compliance program...+ Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data… more
- Sanofi Group (Bridgewater, NJ)
- **Job Title:** Associate Director Global Scientific Communications Immunology Pipeline **Location:** Cambridge, MA or Bridgewater, NJ **About the Job** We ... governing publications globally. The position will report to the Scientific Director on the Respiratory/ Gastroenterology Global Scientific Communications Team.… more
- Novo Nordisk (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions + Serve ... About the Department Our East Coast Global Development Hub brings together the best minds...NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating… more
- IQVIA (Camden, NJ)
- …as outlined by senior management. * May collaborate with other regional and/or global clinical and client teams and other functional leadership to manage ... with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the… more
- Merck (West Point, PA)
- **Job Description** The Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the ... full company Research Laboratories (Research and Development Division) portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling,… more
- Bristol Myers Squibb (Princeton, NJ)
- …Accountable for implementing and supporting strategic information systems that enable Global Development Operations (GDO) function, specifically focusing on Veeva ... Clinical Vault (Veeva CTMS, Veeva eTMF). This role owns...Degree or higher-level education preferred. + Must have Veeva Clinical Vault expertise, with specific knowledge of Veeva CTMS… more
- Fujifilm (Trenton, NJ)
- …The following Manager/supervisor level roles will directly report to the Senior Director Global Quality Systems: Director QA, Associate Director QA, ... **Overview** The Senior Director Global Quality Assurance, Audits &...leadership and team management skills. + Demonstrated knowledge of global GxP practices required - Good Clinical … more
- Merck (Upper Gwynedd, PA)
- …obtain shortest time to approval by global regulatory agencies. + Reports to Associate Vice President, Executive Director , or Senior Director in the ... **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs...Development Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS)… more
- Sanofi Group (Bridgewater, NJ)
- …diseases. **Main Responsibilities:** The Early Pipeline Gastroenterology Associate Medical Director reports to the Global Medical Head of Immunology and ... + Significant immunology, and gastroenterology experience required + Experience in pipeline, clinical development and/or medical affairs on a global or regional… more
- Bristol Myers Squibb (Princeton, NJ)
- …development and implementation of technical solutions for integrating, analyzing and reporting clinical data. Associate Director drives the development and ... implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative relationships and work… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as a Associate Director Medical Writing where you will be responsible for medical ... data presentation and interpretation. In addition to project responsibilities, the Associate Director , Medical Writing is responsible for non-project related… more
- Bristol Myers Squibb (Princeton, NJ)
- …trials. This includes a centralized triage function for informed consent negotiations with global clinical trial sites, IRBs/ECs, and health authorities, as well ... internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role...questions and requests for IC language changes supporting our global clinical trials and will be responsible… more
- System One (King Of Prussia, PA)
- …meets industry and regulatory requirements for clinical trial coding. The Associate Medical Coding Director manages and oversees staff, strategic partners, ... Title: Associate Medical Coding Director Full Time...technology that supports efficient dictionary management processes and with Global Patient Safety and Clinical Development for… more
- Bristol Myers Squibb (Princeton, NJ)
- …centralized monitoring for trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a leadership role with ... the BMS R&D pipeline. This role reports to the Director , External Data Acquisition within GDM and is a...degree preferred **Experience Requirements** At least 7 years of global clinical trial expertise with a focus… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , TA (Therapeutic Area) Analysis Standards Leader is ... across the TA, aligning cross-functionally and driving end to end standards. Associate Director , TA Analysis Standards Leader, independently leads improvement… more