- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- … studies ). + Provide timely and strategic recommendations to clinical development programs by identifying appropriate comparators, target patient populations, and ... As a Director , HEOR you will formulate strategies of our...synthesis projects. Collaborate in the development of observational research studies including claims data, patient-reported outcomes (PRO) studies… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Site Engagement Date: Jul 9, 2025 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: 62405 ... Good knowledge of Drug Development Process. + Excellent understanding of the Clinical Study Process including monitoring. + Very good understanding of the … more
- Merck (West Point, PA)
- …West Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology ... pipelines. As an Associate Director , you will represent QP2 on...teams of experienced scientists to discover and advance the clinical development of novel therapeutic agents for cardiometabolic and… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Position Summary:** The Associate Director , Diagnostic Development will serve as the investigational in vitro ... diagnostic (diagnostic) trial-level expert for global clinical studies where approved diagnostics are needed to support the therapeutic program. The ideal… more
- Otsuka America Pharmaceutical Inc. (Bismarck, ND)
- …preparation for a new drug. + Acts as the signatory on NDA submissions and clinical study and safety documents. + Involved in product life cycle management from ... **Job Description** Otsuka is seeking a Director , Global Clinical Development (GCD), who...research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for … more
- Emory Healthcare/Emory University (Lawrenceville, GA)
- …to the Assistant Director of Animal Resources, Field Station, as well as the Associate Director of Animal Resources. ** Clinical ** + Clinical care of ... veterinary technicians and Emory's ACLAM residency training program. Reporting to the Associate Director of Animal Resources, the Senior Veterinarian provides … more
- Pfizer (Cambridge, MA)
- … study teams and provide statistical expertise in designing clinical trials, developing protocols, writing statistical analysis plans, performing statistical ... input and leadership to cross-functional activities - collaborate with other statisticians, study managers, programmers - for assigned studies and regulatory… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …to evaluate clinical stage programs and opportunities for human genetics studies to aid in the selection of indications or evaluation of safety considerations. ... holder will collaborate with various RGC teams and with pre- clinical and clinical development teams at Regeneron...Generate key research questions and then design and execute studies and analyses to help address these questions, interpret… more
- Boehringer Ingelheim (Ridgefield, CT)
- …our strength and competitive advantage lie with our people. As a SR Associate Director , you will collaborate with other epidemiologists and cross-functional ... (TA) lead provides subject matter expertise to the US Clinical Development and Medical Affairs (CDMA) TA team, contributing...of RWE&EPI. The job holder is responsible for overseeing study projects (NIS, IIS, RWE studies ) around… more
- Sumitomo Pharma (Pierre, SD)
- … Protocols, Informed Consent Forms (ICF), Safety Management Plans (SMP), Clinical Study Reports (CSR), Investigator's Brochures (IB), Investigator communications ... Regulatory safety inquiries. + Represents PVRM on post-marketing product specific and/or clinical study team meetings and governance committees. + Performs… more