- 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
- Merck (North Wales, PA)
- …with a particular focus on obesity and obesity-related metabolic disorders. The Senior Director will manage the entire cycle of clinical development, including ... placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be responsible for** + Evaluating pre- clinical … more
- Merck (West Point, PA)
- …Our company is seeking a highly motivated candidate for the position of Director , Vaccine Drug Product Development. Vaccine Drug Product Development ... **Job Description** Our company is a global health care leader with a diversified portfolio...The Director will report to the Executive Director of Vaccine Drug Product Development, have… 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
- Merck (North Wales, PA)
- …degree (eg, MS, MBA, Ph.D., PharmD) preferred + Experience and knowledge of clinical drug development strongly preferred; including the different phases of ... drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in...our company. ** ** **Position Description/Summary:** The GPAM Associate Director , Project Manager, is a core member of Early… 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
- Merck (West Point, PA)
- **Job Description** The Senior Director of Device Product Stewardship will lead a department of up to 15-20 personnel overseeing technical support and product ... effective and statistically sound CAPA plans and issue resolution. The Senior Director will ensure stewards have the appropriate processes and playbooks, appropriate… more
- Merck (West Point, PA)
- …regulatory expectations and shape, present and defend regulatory documents and submissions. The Director is a skilled quantitative drug developer, with a strong, ... aligned, quantitative and model-informed framework to impact strategies and decisions of drug development teams. Finally, the Director mentors or supervises… 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
