- 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
- 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
- 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
- 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 ... clinical studies as a clinical trial assistant or clinical research associate...for adjudication by the CEC. + Participates with the Associate Director of Research and Quality Outcomes… 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
- 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
- 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
- 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
- Bristol Myers Squibb (Summit, 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
- 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
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Associate Director , Safety Scientist in Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical ... and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments. + Ability to work… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Parsippany, NJ_** Real-World Evidence (RWE) has become a vital complement to the traditional clinical trial in the demonstration of the value and safety of new ... has established a core RWE Analytics group within the Clinical Data Sciences (CDS) - RWE Organization to support...of this group will be fully embedded alongside their Clinical , Real-World Evidence (RWE), Medical Affairs Research (MAR) and… more