- Merck & Co. (North Wales, PA)
- …solutions, tactics and resources to address the opportunities.Collaborating with Global Medical and Scientific Affairs (GMSA), US, Senior Director of Medical ... Job DescriptionJob Description:The Associate Director , Marketing, HPV Scientific Strategy plays a critical role in supporting the HPV vaccine franchise.- The HPV… more
- Merck & Co. (Rahway, NJ)
- …medicines. Our company's oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the ... monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May Be Responsible ForEvaluating pre- clinical and translational… more
- Genmab (Plainsboro, NJ)
- …As part of our expanding US Medical Affairs (USMA) team, Genmab is seeking a Senior Director , USMA Solid Tumor Portfolio. This role will report to the VP/Head ... the delivery of timely, accurate and succinct communication of fair-balanced clinical and scientific presentations to healthcare professionals, both proactively… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated ... critical meetings, and relationships with Key External Experts (KEEs). Contributes to clinical / scientific training of relevant DSI stakeholders on the disease… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated ... clinical study(ies) data to internal and external stakeholdersProvides medical/ scientific training on compound/disease and dose modifications/discontinuations as well… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... science and technology. With more than 120 years of scientific expertise and a presence in more than 20...size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member… more
- Merck & Co. (San Diego, CA)
- …public data resources, to generate novel CDx models that can be deployed in clinical trials. You will also support preparation of regulatory documents in support of ... clinical trials.- In addition, you will be the site...implementing rigorous data analysis practices, aligning resources based on scientific priorities, and mentoring and developing team members. You… more
- Genmab (Plainsboro, NJ)
- …our purpose.Reporting to the VP, Head of Global Drug Safety & PV, the Senior Director , Global Drug Safety & Pharmacovigilance Physician serves as the safety ... of products, including review of individual and aggregate AEs and the scientific literature, preparing safety reports, and communicating changes in the product risk… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- Position SummaryThe Sr. Director of Technical Transfer is responsible for activities related to technology transfer from external and internal customers. This ... aspects of technical transfer including analytical transfer, development studies, clinical supplies, manufacturing scale up, equipment and process qualification,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and ... technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND, IMPD, IB) and marketing applications/supplements… more
