- AbbVie (Branchburg, NJ)
- …Development Plan and is responsible for: + Ensuring alignment between the IEST, and Clinical Trial Team(s) + Developing the proposed clinical milestones with ... Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Clinical Development will have global...the project-related clinical development budget with the Clinical Trial Team and Project Manager +… more
- Kelly Services (Basking Ridge, NJ)
- …monitoring preferred + A minimum of 10 years of progressively responsible clinical trial experience within a pharmaceutical, biotechnology, Contract Research ... Hiring Experts.** No C2C Full-time, perm, direct hire The Clinical Research Associate (CRA) is responsible for...A core understanding of GCP as it relates to clinical trial monitoring + Demonstrate a core… more
- System One (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and ... Role: Clinical Study Associate I Type: 12...information and coordinate with DS Regulatory Operations to post trial information on required public forums (eg.clinicaltrials.gov). Support Fair… 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)
- …of smart systems and optimal approaches to support the end to end clinical trial data lifecycle, from collection through submission. + Holding accountability ... in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, Clinical Data Standards is a...**Experience Requirements** + At least 12 years of global clinical trial expertise and a successful track… more
- Bristol Myers Squibb (Princeton, NJ)
- …clear product vision and strategy for the clinical data ecosystem especially with clinical trial design and data science methodologies to enable clinical ... team! **Position Summary:** We are seeking a highly motivated and detail-oriented Associate Director - Product Manager with broad clinical data experience… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …and authors clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments + Authors and/or reviews documents ... We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the… more
- WuXi AppTec (Plainsboro, NJ)
- **Overview** The Clinical Research Associate III Senior Oncology performs and coordinates aspects of field-based and office-based monitoring and data quality ... specified by project manager or supervisor, including but not limited to mentoring of Clinical Research Associate (CRA) I and II personnel. + Participates in… 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
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may be assigned to support the execution ... assignments from the Clinical Study Lead or Clinical Study Associate Manager. The CSS will...plan + Monitors and updates investigator/site status for the trial , and supports with clinical trial… more
- Hackensack Meridian Health (Edison, NJ)
- …works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. **Responsibilities** A day in the ... on each protocol and each patient participating in a clinical trial protocol in the clinical...SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … 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 leadership role...Acquisition is a leadership role with oversight of external clinical trial data acquisition and integration and… more
- Astrix Technology (Trenton, NJ)
- …space. + Working knowledge of Clinical & Regulatory systems such as Clinical Trial Management System (CTMS), electronic Trial Master Files (eTMF), ... for the sale and growth of Astrix Technology Group's Clinical and Regulatory Consulting services to a portfolio of...representative of those that must be met by an associate to successfully perform the essential functions of this… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …**How you will** **contribute:** + Oversee and direct the work of the Clinical trial disclosure programming team (within the Programming Center of Excellence) ... life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Programming in Cambridge, MA, where you will...Standard code, AI and ML applications). + Collaborate with Clinical Trial Transparency Teams to implement data… 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, ... d raft simple, easy to understand policies specific to medical affairs and clinical trial /research activities that empower the business to execute activities in… 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 reports to...Simplification. + Knowledge of IT systems used to support clinical trial processes and the authoring of… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Research (CESR) projects. Candidates should have a comprehensive understanding of clinical trial management, with firsthand experience managing collaborative ... centered around rare diseases and immune disorders. **Summary:** The Associate Director will lead the execution and lifecycle management...to ensure timely follow-up and resolution of issues. + Clinical Trial Management: Oversee clinical … more
- Bristol Myers Squibb (Princeton, NJ)
- …leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning, ... their personal lives. Read more: careers.bms.com/working-with-us . **Purpose** The Associate Director, Biostatistics is a core member of cross-functional development… more
- Bristol Myers Squibb (Princeton, NJ)
- …leads the development and execution of statistical aspects for one or more clinical trials, including contribution to study trial design, analysis planning, ... treatment we pioneer. Join us and make a difference. **Purpose** The Associate Director, Biostatistics is a core member of cross-functional development teams and… more
- Bristol Myers Squibb (Princeton, NJ)
- …the Quality Module for regulatory submissions to support biologics products regarding: Clinical trial applications; New marketing applications; HA responses & ... current regulatory requirements and expectation for small molecule arketing applications, clinical trial applications for projects, and/or lifecycle changes to… more