- 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 (Tarrytown, NY)
- … 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 (Tarrytown, NY)
- …amendments, IRB/IEC submissions and regulatory submissions * Accountable for timely clinical trial execution, reviewing adverse events, monitoring patient ... therapeutic area preferred, along with relevant industry experience. A minium of 2-3yr ( Associate Director ), 4-8yr ( Director ) prior industry experience 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
- 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
- Pfizer (Pearl River, NY)
- …plan. + Designs clinical studies to meet the stated objectives. Assures that clinical trial objectives fit with the clinical program strategy. + Ensure ... to enable quality, compliance and patient safety at the trial , site and patient level. + Ensures development of...+ Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts… more
- Pfizer (Pearl River, NY)
- …Designs clinical studies to meet the stated objectives of a program. Assures that clinical trial objectives of each study fit with the clinical program ... to enable quality, compliance and patient safety at the trial , site and patient level. + Accountable for the...+ Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts… more
- Pfizer (New York, NY)
- …source data key efficacy variables and analyses. * Perform the analyses of clinical trial data, provide statistical interpretation of results, and collaborate on ... **JOB SUMMARY** The **A** **ssociate** ** Director , Oncology Biometrics** is a skilled biostatistician who...the reporting of clinical trial results to regulatory authorities and… more
- Bristol Myers Squibb (Madison, NJ)
- …Patients, and Payers in accordance with local regulations. **Key Responsibilities** The Associate Director of Medical Communications is accountable for the ... aligned medical communications plans; adjust communications plans in accordance with clinical trial results/milestones and changes in the healthcare landscape… more
- Pfizer (Pearl River, NY)
- …into country feasibility. **Support study team** + With supervision of medical monitor ( director /Sr director ) provides clinical input to protocol/study team ... + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts...etc. + **Supports the program team:** + Under supervision ( director /Sr director ) authors clinical sections… 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
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …and/or pharmacologic) studies as per clinical strategy; Reviews, edits and finalizes clinical trial plans + Responsible for the relevance and accuracy of ... System, Neuromuscular and Muscular Diseases. **As a Senior Medical Director , a typical day may include the following:** +...academic clinical trials (10 years post fellowship clinical and research experience, associate or full… 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
- 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
- AbbVie (Florham Park, NJ)
- …substantial understanding of relevant therapeutic area required. + Knowledge of clinical trial methodology, regulatory requirements governing clinical ... in Florham Park, NJ preferred. Will consider remote candidates. Purpose: The Associate Scientific Director , Psychiatry Pipeline role provides medical and… more
- AbbVie (Florham Park, NJ)
- …Experience in Parkinson's and/or Movement Disorders is preferred. + Knowledge of clinical trial methodology, regulatory requirements governing clinical ... onsite) in Florham Park, NJ preferred. Will consider remote candidates. The Associate Scientific Director provides medical and scientific strategic and… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on ... you are interacting with CROs in the management of ex-US/ex-EU CTAs towards clinical trial activations preferred + If you have a high attention to detail;… more