- Lilly (Branchburg, NJ)
- …for this position is $111,000 - $162,800 **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
- Bristol Myers Squibb (Princeton, NJ)
- …and implementation of innovative strategies and technologies for clinical trial programming. Associate Director develop collaborative relationships and ... development and implementation of technical solutions for integrating, analyzing and reporting clinical data. Associate Director drives the development… 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
- Takeda Pharmaceuticals (Trenton, NJ)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Patient Safety Clinical Operations in Cambridge, ... skills in negotiation and consensus decision making. + Expert knowledge of clinical trial and Pharmacovigilance methodologies including detailed comprehension of… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …innovation-driven company to inspire you and empower you to shine? Join us as an Associate Director , GCP Compliance based remotely reporting to the Director , ... of compliance management related to quality events and internal audits for clinical trial delivery functions including the identification and development of… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Data Configuration Engineer in our Cambridge, MA office. At Takeda, we ... team, provides strategic planning, integrating, execution, build and oversight of clinical trial deliverables. CDCS leads the integration of collected… more
- Penn Medicine (Plainsboro, NJ)
- …to day operations of clinical research proposals for their team. The Associate Director will work with Investigators and data informatics teams/programs to ... living your life's work? We are hiring for an Associate Director Oncology Research Operations to join...Specialist, Billing Compliance staff, and Finance office to develop clinical trial budgets. Communicating any specialized study… 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
- Merck (Trenton, NJ)
- **Job Description** The Regional Medical Scientific Associate Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in ... Research, Scientific Congress Support, and Scientific Insights. Regional Medical Scientific Associate Director 's liaise between the scientific community and the… 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
- Taiho Oncology (Princeton, NJ)
- Associate Director , Biostatistics Princeton, NJ, USA Req #421 Monday, December 23, 2024 Looking for a chance to make a meaningful difference in the oncology ... Summary: + This position will have direct responsibility including clinical trial design and execution, analysis and...data, and authoring/review of scientific and regulatory documents. The Associate Director of Biostatistics will have CRO… more
- Merck (Trenton, NJ)
- **Job Description** The Regional Medical Scientific Associate Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in ... SL inquiries on issues outside of Regional Medical Scientific Director scope (eg, grants) to appropriate company resources consistent...to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study… 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
- Takeda Pharmaceuticals (Trenton, NJ)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Signal Management Process Excellence in Cambridge, MA, where ... experience in pharmacovigilance + In depth knowledge and experience of clinical trial methodology, pharmacovigilance regulations, signal detection and… more
- Bristol Myers Squibb (Princeton, NJ)
- …synopses and protocols. Contribute in cross-functional rapid response teams to respond to Clinical Trial Application (CTA) queries on new protocols and protocol ... coordination with clinical plans and marketing objectives. + Experience with clinical trial assays (CTA) in drug clinical trials in communicating between… more
- Novo Nordisk (Plainsboro, NJ)
- …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions + Serve as a… more
- Bristol Myers Squibb (Princeton, NJ)
- …across a matrix. * Experience with drug development, commercialization, and healthcare, clinical trial management a plus. **\#LI-Hybrid** If you come across ... Cell Therapy (CT) Organization. **Details** This role reports directly into the Senior Director of Strategy and Operations and will be a strategic and operational… more
- Bristol Myers Squibb (Princeton, NJ)
- …literature, regulatory and HTA documents to develop an understanding of the clinical , regulatory/HTA and commercial climate. + Contributes to preparation of the ... price negotiation. + Contributes to the design of innovative and efficient clinical trials, including the selection of study population/endpoints to address study… more
- Novo Nordisk (Plainsboro, NJ)
- …(phase I trials) + Provide safety input to Product Development Plan (PDP), Trial Outline, Protocol, Clinical Trial Report, Investigator's Brochure (IB), ... and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct… more