- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Director , Clinical Pharmacology actively contributes to multi-disciplinary teams by providing innovative ... interpreting study data and effectively communicating findings to a broad audience. The Director , Clinical Pharmacology will be relied upon to act independently,… more
- Organon & Co. (Jersey City, NJ)
- …affairs, safety and pharmacovigilance, Chemistry, Manufacturing and Controls (CMC), medical affairs and business development. Non- Clinical Safety Assessment ... **Job Description** **The** **Position** The Non- Clinical Safety Assessment Representative within the Non- Clinical Development (NCD) team, is accountable for the… more
- Organon & Co. (Jersey City, NJ)
- …early development plans. The Clinical Pharmacology Lead will serve as the medical monitor and/or study director responsible for the execution (in conjunction ... **Job Description** **The** **Position** The Director , Clinical Pharmacology Lead will be... will work collaboratively with cross-functional colleagues in preclinical science , data science , clinical operations,… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Director , Biopharmaceutics will provide expert biopharmaceutical guidance on the pharmacokinetic performance of ... the general medicines portfolio of products marketed worldwide. The Associate Director , Biopharmaceutics will also be responsible for contributing to and reviewing… more
- Organon & Co. (Jersey City, NJ)
- …Dermatology Outcomes Research Epidemiology and Economics will report to the headquarters Director of Medical Affairs Outcomes Research. Focusing on Dermatology, ... issues. Customer, Market, and Competitor Insights + Develop an understanding of science , medicine, clinical practice, and therapeutic areas to address customer… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Medical Director , Clinical Sciences functions as clinical leader of a section of a clinical program (eg, an indication, a new formulation, or ... a specific development phase), under leadership of Program Lead Medical Director (Program Lead MD) or Sr. Medical Director . A day in the life may include… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Executive Medical Director , Clinical Sciences , Obesity is responsible for effectively managing obesity opportunities in an end-to-end framework ... (CDU) for assigned program(s) / asset(s). A typical day in the life of an Executive Medical Director may include the following: + Leads the Global Clinical … more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Senior Medical Director , Clinical Sciences is responsible for facilitating assigned studies, providing investigator support of Regeneron driven ... and conduct issues. This role reports into the Clinical Program Lead, Clinical Sciences ...academic/ clinical setting may be considered at the Medical Director level. A typical day in… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- The Medical Director , Clinical Sciences , Oncology is a qualified physician scientist with exceptional academic clinical trials' experience, ... preferably in solid tumor Oncology drug development. The Medical Director drafts designs of clinical study concepts which lead to clinical trial… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …late phase development. Reports to the Sr Dir/ Director , Clinical Science , Internal Medicine and collaborates closely with Medical Director (s) (MDs) ... The Associate Director , Clinical Sciences contributes...Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …(univariate and multivariate). The student will work closely with the global program head, medical director and clinical pharmacology director during the ... If you're currently a medical school student interested in drug discovery and...a fit for an internship in our Internal Medicine Clinical Development Unit. **In this role, a typical internship… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …centric, science focused company. Reporting to the Vice President of Global Medical Strategy and Operations, the Senior Director , Medical Education & ... PROTECTION ACT (http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf) YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Gilead Sciences will not discharge… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …to join the **Patient Safety Strategic Operations** team as an **Associate Director , Patient Safety Medical Device Safety** responsible for supporting activities ... and ensure operational excellence through successful business partner collaboration. The Associate Director , PS Medical Device Safety will be a medical… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …PROTECTION ACT (http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf) YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Gilead Sciences will not discharge ... Join Gilead and help create possible, together. **Job Description** The **Associate Director , USMA Strategic Execution** will play a critical role in the… more
- Guidehouse (New York, NY)
- …Business or related course of study. + 7-10 years of Life Sciences (Pharmaceutical, Biotech, Specialty Pharma and/or Medical Technology) consulting experience ... **:** None **What You Will Do** **:** Is life sciences in your DNA? Breakthroughs in pharma are helping...Science industries. + Ability to grasp and communicate clinical and business implications of technically complex products and… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …into actionable insights and tactical plans. + Ability to understand and communicate clinical data and high-level science . The salary range for this position ... PROTECTION ACT (http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf) YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Gilead Sciences will not discharge… more
- Guidehouse (New York, NY)
- …Business or related course of study. + 10 years of Life Sciences (Pharmaceutical, Biotech, Specialty Pharma and/or Medical Technology) consulting experience ... program design, implementation, and monitoring services to pharmaceutical, biotechnology, and medical device, companies. We support our clients across the lifecycle… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …PROTECTION ACT (http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf) YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Gilead Sciences will not discharge ... Join Gilead and help create possible, together. **Job Description** As an Associate Director , Global Regulatory Affairs, you will act as the Regional Regulatory Lead… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …PROTECTION ACT (http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf) YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Gilead Sciences will not discharge ... project manager in Product Launch & Change Planning (PLCP) within Global Clinical Supply Chain (GCSC), overseeing and allocating project managers to product… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …and Medical Affairs launch planning. + Partner across Public Affairs, Medical Affairs, Market Sciences , Clinical Development, Legal, Ethics and ... PROTECTION ACT (http://www.dol.gov/whd/regs/compliance/posters/eppac.pdf) YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT Gilead Sciences will not discharge… more
