- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …disorders. Summary This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational ... leadership on product labeling in collaboration with Global Regulatory Leads (GRLs). This position may serve as an ad hoc member of Global Project Team (GPT)… more
- Catalent (Manassas, VA)
- Associate Director , Regulatory Affairs Position Summary: Catalent is a global , high-growth, public company, and a leading partner for the pharmaceutical ... consumer and Catalent employee. The primary duty of the Associate Director , Regulatory Affairs is...offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development team ... Company Information Legend Biotech is a global biotechnology company dedicated to treating, and one...cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at ouor company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This ... Associate Director will work with scientists within QP2 by applying...other pharmacometric analyses-Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… more
- Merck & Co. (Rahway, NJ)
- …completion of carefully designed clinical trials is critical to drug development.The Associate Director , Clinical Trials Communications role within our Research ... enterprise wide (Internal and External) critical communications, focused on our global Clinical Trial efforts.This role is responsible for supporting the… more
- Merck & Co. (North Wales, PA)
- …Under the direction of the Program Lead, you will collaborate with global , cross-functional team members including clinical directors and study managers to ... trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates in the… more
- Aequor (Newbury Park, CA)
- …and develop solutions. Provide Subject Matter Expertise in Veeva Vault Configuration and Regulatory Processes to a global user base. Develop and deliver training ... materials and presentations to a global audience. Author/review/approve quality Regulatory Information Management & Systems documents Analysis of the existing… more
- Merck & Co. (North Wales, PA)
- …in patients who need it most. Invent. Impact. Inspire.Our company is a global health care leader with a diversified portfolio of prescription medicines, vaccines and ... you collaborate with copy, design, UX, architecture, internal legal, medical and regulatory teams in the co-design, co-creation, and execution of campaign plans… more
- Eisai, Inc (NJ)
- …If this is your profile, we want to hear from you. Job Summary The Associate Director , Clinical Outsourcing, will oversee and lead and support activities related ... development.#LI-TS1Eisai Salary Transparency Language:The base salary range for the Associate Director , Clinical Outsourcing is from :157,200-206,300Under… more
- Merck & Co. (Rahway, NJ)
- …products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional ... integration of the device development activities with the clinical, regulatory , formulation, commercial and other key company functions.Represent Device Development… more
- Eisai, Inc (Nutley, NJ)
- …experience with/using the following (which may have been gained concurrently): Supporting Regulatory and/or Safety functions in a global environment; Supporting ... aligns with infrastructure, security and/or corporate systems' roadmaps. Collaborate with global finance for the planning, approval and reporting of budgets and… more
- Merck & Co. (Rahway, NJ)
- …configuration for the SAP FI/CO modules.- This role reports to the Global Financial Business Management Director . Responsibilities: Leadership and Management: ... drive revenue and productivity, thereby advancing our company's contribution to global medical innovation.Enterprise IT (EIT) is an essential component of the… more
- Merck & Co. (Millsboro, DE)
- …Millsboro Delaware seeks to add an Attending Veterinarian in the role of Associate Director .This position will have overall responsibility for oversight and ... DEA, DNREC, etc.) of animal facilities and program reviews is required.PurposeThe Associate Director /Attending Veterinarian will report to the Site Quality Head/… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical Development, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Merck & Co. (Rahway, NJ)
- …company, the successful applicant will play a critical role in leading major global initiatives aimed at enhancing Medical Affairs practices. The SRO is a recognized ... initiatives.Responsibilities:Support the SRO Lead in the execution of extensive, global initiatives, ensuring the program objectives and timelines are consistently… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …an equal opportunity employer including veterans and people with disabilities.SummaryThe Associate Director will be responsible for developing and implementing ... hands on population PK and PKPD analyses and participate in regulatory interactions and submissions representing the Clinical Pharmacology and Pharmacometrics/… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …to date- Support regulatory inspection related activities as required- Support Head, Global strategy and operations to develop and plan the Global QA ... people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi...responsibility to collaborate with, and support the head of Global QA strategy and operations. In this position, the… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of ... Company Information Legend Biotech is a global biotechnology company dedicated to treating, and one...Operations team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …equal opportunity employer including veterans and people with disabilities. Summary The Associate Director , External Data Management, is accountable for the ... the data services they provide to support drug development processes and global submissions. This position provides expertise within Data Management by partnering… more
