- Lilly (Branchburg, NJ)
- …life better for people around the world. **Position Description:** The Clinical Trial (CT) Supply Management Associate Director will provide operational ... to improve performance and speed drug development. **Responsibilities:** + Deliver improved clinical trial supply chain performance, assess and mitigate risk,… more
- Actalent (Basking Ridge, NJ)
- …This role is primarily a tactical study delivery role, reporting into an Associate Director or above responsible for Operational Study Strategy. Responsibilities ... Job Title: Clinical Study ManagerJob Description The incumbent will be...audit activities. + Provide oversight of the transmittal of trial and site-level documents to the Document Control Center… more
- Merck (Rahway, NJ)
- **Job Description** **Position Description:** ** Associate Director , Clinical Scientist** This position drives scientific planning, strategy and execution of ... team members including clinical directors and study managers to lead/support clinical trial scientific activities. Job Responsibilities + Responsible for the… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- … Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the development, evaluation, ... scientific integrity and interpretation of study data of a clinical development program. The Associate Director...clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments + Authors… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Precision Medicine Clinical Laboratory Operations will be responsible for Clinical Laboratory Project & Program management for ... be done in collaboration with Precision Medicine Strategy Leads, Clinical Trial Management, Clinical Laboratory...early and late-stage programs within our pipeline. **As an Associate Director , a typical day may include… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Clinical Sciences contributes to the development, evaluation, planning and execution of hematology clinical studies and ensures ... on clinical studies and programs. As an Associate Director , a typical day may include...clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments. Authors and/or… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... + Study Planning and Execution: Provides input on major milestones of trial , clinical trial plan and contingency planning; Analyzes and updates management… more
- Bristol Myers Squibb (Madison, NJ)
- …. **Position Summary** Global Data Management (GDM) is responsible for clinical trial data acquisition, data standards governance, data management, ... trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a...Acquisition is a leadership role with oversight of external clinical trial data acquisition and integration and… more
- Bristol Myers Squibb (Madison, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . The ** Associate Director , Development Strategy Analyst** is an experienced clinical research ... professional skilled in analyzing clinical trial data. They use this expertise to assess study... trials. Key demonstrated competencies for the **A** **ssociate Director level** include: + Organizational Impact: Increased sphere of… more
- Mount Sinai Health System (New York, NY)
- …safety aspects of clinical research trial (s). Under guidance of the Associate Director of Research and Quality Outcomes, the CRA is responsible for ... clinical studies as a clinical trial assistant or clinical research associate...for adjudication by the CEC. + Participates with the Director of Research and Quality Outcomes in the preparation,… more
- Bristol Myers Squibb (Madison, NJ)
- …This includes a centralized triage function for informed consent negotiations with global clinical trial sites, IRBs/ECs, and health authorities, as well as ... internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role...Simplification. + Knowledge of IT systems used to support clinical trial processes and the authoring of… more
- Merck (Rahway, NJ)
- **Job Description** The Associate Director , Business Analyst, within Metrics, Analytics & Performance (MAP) will lead activities related to the development, ... and monitor performance across our portfolio, studies & processes within Global Clinical Trial Operations (GCTO). **Primary responsibilities include but are not… more
- Bristol Myers Squibb (Berkeley Heights, NJ)
- …every treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director , Biostatistics is a core member of cross-functional development ... leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning,… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director , Vendor Management, is responsible for assessing, onboarding, and overseeing the health and performance of vendors involved in clinical ... reviews and updates of business continuity plans. + Ensure minimal disruption in clinical trial operations through effective continuity planning. + Contribute to… more
- IQVIA (Newark, NJ)
- …(SES) is a unique service providing site-based clinical research staff to trial sites globally. Reporting to the Director , Head of Project Delivery within ... and development of new SES services. In addition, this Associate Director role will be a key...Collaborate with cross-functional project leads within PSCS (Patient Recruitment, Clinical Trial Educators, Decentralized Trials, etc.) to… more
- Bristol Myers Squibb (Madison, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director , WW Cell Therapy Medical, Operations and Product Science ... will report to the Executive Director CT Medical Franchise. He/she will expected to attend...CAR T products including taking the role as the clinical trial physician as indicated. He/she will… more
- AbbVie (Florham Park, NJ)
- …substantial understanding of relevant therapeutic area required. + Knowledge of clinical trial methodology, regulatory requirements governing clinical ... level will be determined by the qualifications listed below. Purpose The Associate Scientific Director provides medical and scientific strategic and operational… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …on real-world evidence, and creating hope for all facing illness. The Associate Director , Biostatistics is responsible for providing statistical support to ... + Excellent statistical knowledge and project planning skills + Knowledge of clinical trial research and regulatory requirements + Familiarity with SDTM/AdaM… more
- Pfizer (New York, NY)
- …communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results **,** ... biostatistics, or related field. + A minimum of 4 years' experience in the clinical trial setting (preferably in oncology of Pharma). + Relevant clinical … more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Join Gilead and help create possible, together. **Job Description** ** Associate Director , Biostatistics** **Position Overview:** Biostatisticians at Gilead ... data in efficiently achieving regulatory, scientific and business objectives. The Associate Director will be primarily responsible for the business,… more