- Genmab (Plainsboro, NJ)
- …and authentic is essential to fulfilling our purpose.The RoleGenmab is searching for an experienced Director , Global Clinical Drug Supply to be part of ... at the forefront of bringing medicines to cancer patients and other serious diseases. Director , Global Clinical Drug Supply will work in partnership with… more
- Genmab (Plainsboro, NJ)
- …collaboration, excellence, and a can-do attitude to achieve results.You will be reporting to Director , Global Clinical Drug Supply in Copenhagen, ... an experienced Senior Clinical Drug Supply Manager to join our Global Clinical Drug Supply Operations team.As Senior Clinical Drug Supply… more
- Genmab (Plainsboro, NJ)
- …to be our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Clinical Trial Manager (GCTM) is accountable for the end-to-end delivery ... of a single or multiple clinical trials from strategy outline through to CSR by...CPL in a timely mannerExecute operational strategies related to drug supply, regulatory submissions, and recruitmentBudget and PlanningAssist in… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/Associate Director will be responsible ... Regulatory Affairs (GRA) and will report to the Sr Director , Labeling, Policy and Intelligence. The position will be...global regulations and guidance as they relate to global labelingUnderstanding of clinical development of novel… more
- Genmab (Plainsboro, NJ)
- …needs of the US healthcare market through collaboration with US Commercialization, Global Medical Affairs, Clinical Development, Regulatory, and other cross ... disease area expert in both internal and external venues including the US/ Global cross-functional teams, clinical development teams, advisory boards, steering… more
- Genmab (Plainsboro, NJ)
- …for new trials to ensure efficient and effective trial operations.Point of Contact for Global Clinical Trial Managers: Act as the primary point of contact, ... essential to fulfilling our purpose.The Role & DepartmentThe Associate Director , Vendor Management, will play a pivotal role in...a pivotal role in managing the relationships with the clinical vendors as well as coordinate and manage outsourcing… more
- Ascendis Pharma (Princeton, NJ)
- …offer a dynamic workplace for employees to grow and develop their skills. The Director , Global Head of Publication Planning is responsible for leading the ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...of Patients, Science, and Passion, we use our TransCon(R) drug development platform to fulfill our mission of developing… more
- Novo Nordisk (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions + Serve ... preferred + Minimum of 8 years total pharmaceutical/related industry experience in drug development required + Demonstrated knowledge of global regulatory… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the ... of labeling content and strategy of multiple assigned products in various stages of drug development, which may include one high complexity product and updates to or… more
- Bristol Myers Squibb (Princeton, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Early Clinical Development function is part of a global scientific organization ... molecules, biomarkers, and mechanistic hypotheses in humans. The group drives early clinical strategy, and the design, execution, and interpretation of studies to… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …is true to the best of my knowledge. **Job Description** **OBJECTIVES:** Global Evidence and Outcomes (GEO) contributes to the successful development and ... new and innovative therapies. Assigned to one or more global product(s), or as the lead for a disease...GEO, this role informs and contributes to product strategies, clinical development plans and leads the development and execution… more
- Bristol Myers Squibb (Princeton, NJ)
- …and/or Psychiatric** **Key Competency Requirements:** + Advanced knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations + ... at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Clinical Science Lead reports through the Clinical Science function which… more
- Bristol Myers Squibb (Princeton, NJ)
- …through all stages of a products lifecycle. Members of the organization develop global regulatory CMC strategies and partners with key stakeholders to execute the ... Medical Information to build/maintain database to address external questions regarding drug products. **Position Summary / Objective** Oversee management of multiple… more
- Novo Nordisk (Plainsboro, NJ)
- …within the liver disease team working with MASH and/or ALD projects covering clinical drug development from preclinical assessment through Phase 1-4. In doing ... We are building a multi-talented team of physician scientist drug developers that works together to tackle key challenges...clinical development problems + Work with the larger Global Project Team to deliver excellent medical support for… more
- Merck (Trenton, NJ)
- …rapidly to changing situations/environment. + Knowledge in ophthalmology and/or cardiometabolic clinical drug development programs + Knowledge in modeling of ... small molecules, biologics and non-traditional therapeutics like peptides, novel biological The Director is a skilled quantitative drug developer, with a strong,… more
- Novo Nordisk (Plainsboro, NJ)
- …Qualifications + MD or the international equivalent is required + 4+ years of clinical drug development experience from the pharmaceutical or biotech industry + ... or industry. In this role, the Senior International Medical Director will be the medical lead for clinical...clinical development program as medical lead and expert drug developer, providing input and guidance to both internal… more
- Taiho Oncology (Princeton, NJ)
- Sr. Director , PV Medical Surveillance Princeton, NJ, USA Req #378 Monday, July 15, 2024 Looking for a chance to make a meaningful difference in the oncology space? ... guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are… more
- Merck (Trenton, NJ)
- …and Oncology Translational Studies Program (OTSP) research studies. **Upon request from Global Clinical Trial Operations (GCTO):** + Identify barriers to patient ... about any drug , vaccine, or biologic product._ Regional Medical Scientific Director _have no sales objectives or accountability for prescribing or sales of any… more
- Merck (Trenton, NJ)
- …team in the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects ... strategic elements of drug development. As a subject matter expert, the Director within the QP2-IO Group will work closely with teams of highly collaborative,… more
- Sumitomo Pharma (Trenton, NJ)
- …for the position of **Associate Director , Regulatory Affairs** . The Associate Director is part of the Global Regulatory Affairs (GRA) team based in ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
