- 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
- AbbVie (Branchburg, NJ)
- …Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Clinical Development will have global or ... Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director ,...responsible for: + Ensuring alignment between the IEST, and Clinical Trial Team(s) + Developing the proposed… 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...and optimal approaches to support the end to end clinical trial data lifecycle, from collection through… 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
- 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 (Princeton, NJ)
- …**Position Summary:** We are seeking a highly motivated and detail-oriented Associate Director - Product Manager with broad clinical data experience to join ... vision and strategy for the clinical data ecosystem especially with clinical trial design and data science methodologies to enable clinical data… more
- Bristol Myers Squibb (Princeton, NJ)
- …more: careers.bms.com/working-with-us . Global Data Management (GDM) is responsible for clinical trial data acquisition, data standards governance, data ... 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 (Princeton, NJ)
- …strong working knowledge of Pharmaceutical R&D business processes, particularly in Clinical Trial Operations, with demonstrated command of key concepts, ... enable Global Development Operations (GDO) function, specifically focusing on Veeva Clinical Vault (Veeva CTMS, Veeva eTMF). This role owns end-to-end responsibility… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Programming in Cambridge, MA, where you will oversee and ... & Quantitative Sciences team, you will report to the Director , Programming. Takeda SQS is looking to add individuals...**contribute:** + Oversee and direct the work of the Clinical trial disclosure programming team (within the… more
- Bristol Myers Squibb (Princeton, NJ)
- …Include : + Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data analytics, ... their decisions. + Under the direction of the Senior Director , US and Above Market Medical and Market Access...easy to understand policies specific to medical affairs and clinical trial /research activities that empower the business… more
- Bristol Myers Squibb (Princeton, 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
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders. **Summary:** The Associate Director will lead the execution and lifecycle management of ... Research (CESR) projects. Candidates should have a comprehensive understanding of clinical trial management, with firsthand experience managing collaborative… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Purpose** The Associate Director , Biostatistics is a core member of cross-functional ... leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning,… more
- Bristol Myers Squibb (Princeton, 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
- 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
- Bristol Myers Squibb (Princeton, NJ)
- …**Summary/Scope** Reporting to Senior Scientific Director Translational Medicine (TM), the TM Associate Director will be part of the late stage TM group. The ... stage drug development and activities required for and related to clinical trial initiation, maintenance and completion + Strong verbal and written communication… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …to the best of my knowledge. **Job Description** **About the role:** ** Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology ... you will be a vital contributor to our inspiring, bold mission. As an Associate Director in the Nonclinical Regulatory Writing and Systems (NRWS) Department… more
- Bristol Myers Squibb (Princeton, NJ)
- …stage drug development + Experience in activities required for and related to clinical trial initiation, maintenance and completion + Experience in interacting ... Join us and make a difference. **Summary/Scope** Reporting to Senior Scientific Director Translational Medicine, the TM Sr. Principal Scientist will be part of… more
- Bristol Myers Squibb (Princeton, NJ)
- …matrixed environment and managing external agencies; generating, analyzing and interpreting clinical trial and published data; and scientific communication and ... Read more: careers.bms.com/working-with-us . Employer: Bristol-Myers Squibb Company Position: Associate Medical Director , Eliquis Worldwide Medical Affairs… more
- Bristol Myers Squibb (Princeton, NJ)
- …the development and implementation of innovative strategies and technologies for clinical trial programming + Independently develops, validates, troubleshoots, ... towards industry experience + Proficient knowledge of drug development process, clinical trial methodology, regulatory guidance, industry standards, statistical… more