- 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 (New York, NY)
- … clinical trial populations. This role will report into the Associate Director , Diversity & Patient Inclusion. Responsobilties: + Drive the strategic ... required by the FDA for all clinical studies (PhIII) to improve clinical trial diversity. With this role, you will be an important member of the team… 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 (Berkeley Heights, 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
- Bristol Myers Squibb (Madison, NJ)
- …Summary / Objective** + Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial ... team members + May support clinical development planning (collaboration with Clinical Development Lead/ Clinical Trial Physician for provision and… 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
- Gilead Sciences, Inc. (Parsippany, NJ)
- …specializes in process improvements, procedural documents, and quality and inspection readiness for Clinical Operations. The Associate Director , will be a ... Join Gilead and help create possible, together. **Job Description** The Clinical Trial Capabilities (CTC) organization offers infrastructure, support, and… more
- The 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 ... for adjudication by the CEC. + Participates with the Associate Director of Research and Quality Outcomes... clinical studies as a clinical trial assistant or clinical research associate… 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
- AbbVie (Florham Park, NJ)
- …etc.) at the regional/local level. + Participation in design and execution of clinical trial safety, product safety and risk management plans. Responsible for ... substantial understanding of relevant therapeutic area required. + Knowledge of clinical trial methodology, regulatory requirements governing clinical … more
- AbbVie (Florham Park, NJ)
- …Completion of a subspecialty fellowship is desirable. + At least 2 years of clinical trial experience in the pharmaceutical industry, academia, or equivalent. + ... to support a global scientific and business strategy. + Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …on real-world evidence, and creating hope for all facing illness. The Associate Director , Medical Affairs, Movement Disorder/Parkinson's Disease will be ... (ND0612) and related diseases in close collaboration with cross-functional colleagues. The Associate Director , Medical Affairs will serve as a subject matter… 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
- Merck (Rahway, NJ)
- …the **Quantitative Pharmacology and Pharmacometrics -** **Immune/Oncology** team in the role of Associate Director . The team is part of the Global Clinical ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the Group will work closely with teams of… 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
- AbbVie (Newark, NJ)
- …@abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director , Patient Experience Data (PED) Policy & Best Practices, ... areas for AbbVie in alignment with external policy and scientific advancements. The Associate Director , PED Policy & Best Practices, will cultivate strong… 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
- 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
- Bristol Myers Squibb (Madison, NJ)
- …more: careers.bms.com/working-with-us . **Position Summary** The Market Access/HEOR GBDS Associate Director provide statistical support to Market Access/HEOR ... market access and price negotiations. With appropriate experience, the Associate Director can take a lead role...and HTA documents to develop an understanding of the clinical , regulatory/HTA and commercial climate. + Contributes to preparation… more