- Daiichi Sankyo, Inc. (Bernards, NJ)
- …oversight groups for case processing activities and reports to the Director of PV Case Management .Responsibilities:ICSR Processing: Oversees QC activities, ... with CROs, vendors, and partners; and participates on interdepartmental study teams. This level handles escalated global CSPV case...supports projects and interacts with the DSI Case Management team / global case management team… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …This position will require line management responsibility of Directors, Associate Directors, Clinical Study Managers, who are primarily responsibility for ... and overall delivery and tactical execution of the clinical studies . The senior director will ensure a...Lead will be able to appropriately manage resources across Study Management resources to ensure flexible resourcing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Associate Director Global Medical Affairs Oncology (GMA), under the direction ... of the Senior Director / Director , GMA Oncology (Global Medical Affairs team...as medical lead for select company-sponsored GMA evidence generating studies /projects. Manages all medical aspects such as study… more
- Insmed Incorporated (San Diego, CA)
- …for Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Associate Director , EDC Programming will lead and oversee EDC ... support clinical trials, ensuring data quality, compliance, and efficiency throughout the study lifecycle. The AD, EDC Programming will perform optimized EDC builds… more
- Eisai, Inc (Nutley, NJ)
- …make a difference. If this is your profile, we want to hear from you. The Associate Medical Director , US Oncology Medical Affairs - Women's Cancer assists in the ... development within the Medical Affairs department for assigned product(s). The Associate Medical Director utilizes expert medical, clinical and scientific… more
- Merck & Co. (Upper Gwynedd, PA)
- …science that radically changes the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology ... Clinical Research Group. Under the guidance of a supervisor, the Senior Director has primary responsibility for the planning and directing of clinical research… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryAssociate Director , Global Medical Affairs Oncology Publications works with GMA Oncology ... Liaise with internal external authors, academic research organizations, and study investigators- Manage vendor budget and activities- Oversee the quality… more
- Humana (Lansing, MI)
- **Become a part of our caring community and help us put health first** The Associate Director , Care Management , will provide oversight to ensure Humana's ... with the Chief Medical Officer, Quality Improvement Director , Utilization Director , Population Health Management Director and National Medicaid… more
- Takeda Pharmaceuticals (Lexington, MA)
- …company to inspire you and empower you to shine? Join us as an Associate Director , Vendor Management (Clinical Supplies) based in Lexington, MA ... will be a necessary contributor to our inspiring, bold mission. **GOALS:** + The Associate Director , Vendor Management (Clinical Supplies) is responsible for… more
- J&J Family of Companies (Irvine, CA)
- …more at https://www.jnj.com/medtech We are searching for the best talent for an ** Associate Director , Project Management ** ( **Clinical Research)** to ... practices. + Serve as a subject matter expert in the program and project management of clinical study development and execution. + Guide and mentor project… more
- CBRE (Vega Baja, PR)
- Associate Project Management Director - Life Sciences Job ID 211624 Posted 31-Mar-2025 Service line GWS Segment Role type Full-time Areas of Interest ... Construction, Project Management Location(s) Bayamon - Puerto Rico - United States...Preferred experience in regulated areas such as imaging, animal studies , laboratories, environmentally-controlled areas, and production areas thus the… more
- Takeda Pharmaceuticals (Boston, MA)
- …will inspire you and empower you to shine? Join us as a PV Risk Management Scientist/ Associate Director . At Takeda, we are transforming the pharmaceutical ... strive for excellence in everything we do. As an Associate Director / PV Risk Management ...the patient's perspective into benefit-risk activities (eg patient preference studies ) + Collaborate with Safety Leads, Clinical Leads, PV… more
- Regeneron Pharmaceuticals (Armonk, NY)
- Regeneron Pharmaceuticals has an exciting new opportunity as an Associate Director , Diagnostics Project Management & Delivery **In this role, a typical day ... might include:** The role of Associate Director , Diagnostics Project Management ...and CDx regulatory activities against clinical drug development and study timelines + Review clinical protocols, informed consent documents… more
- Stanford University (Stanford, CA)
- Associate Director , Capital Planning and Space Management **Land, Buildings and Real Estate, Stanford, California, United States** Administration Post Date ... the University. **Who you are:** The Associate Director of Capital Planning and Space Management ...with the Diversity and Access Office and Districts Project Management . Communicate capital planning, study , project, policy… more
- AbbVie (Chicago, IL)
- …Management (CSM) including Area Head Study Start-up, Area Head Site Management , Area/Region/country leadership, TA Director - Global Site Management * ... . Job Description This person reports into the Therapeutic Area (TA) Director , Global Site Management and is responsible for managing 3… more
- AbbVie (North Chicago, IL)
- …Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose The Associate Director - eQMS (electronic Quality Management System) Technologies is ... biologics, combination products and medical devices reporting into the Director , eQMS Technologies. Responsibilities: *Business system owner (BSO) of validated… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …and help create more tomorrows. **Job Description** + The ** Associate Director , Planisware Clinical Trial Planning, Resource Management , and Reporting** is a ... 1.) accuracy of the critical path timelines for multiple studies within a product and accurate representation of the...and clinical plans + update project templates and styles.Resource Management & Reporting: + Support Director of… more
- Sumitomo Pharma (Augusta, ME)
- …seeking a dynamic, highly motivated, and experienced individual for the position of ** Associate Medical Director .** The Associate Medical Director ... subject matter expert (SME) on behalf of PVRM for: Study Protocols, Informed Consent Forms (ICF), Safety Management... Study Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR),… more
- Lilly (Indianapolis, IN)
- …are determined to make life better for people around the world. Purpose: The Associate Director / Director , Clinical Trial Foundations (CTF), will serve as the ... on the strategies, integrations, and improvements for systems and capabilities. The Associate Director / Director is responsible for collaborating with… more
- Bristol Myers Squibb (Princeton, NJ)
- …trials and directly contributes to the BMS R&D pipeline. This role reports to the Associate Director , eCOA Management within GDM and is a full-time, ... lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Manager, eCOA Management role is essential to the study level operationalization… more
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