- Merck & Co. (Rahway, NJ)
- …medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of ... may be responsible for: -Analyzing and summarizing the clinical findings from studies to support decisions...study of marketed compounds. In executing these duties, the Director may: Supervise the activities of Clinical … more
- Genmab (Plainsboro, NJ)
- …authentic is essential to fulfilling our purpose.The RoleGenmab is searching for an experienced Director , Global Clinical Drug Supply to be part of Global ... at the forefront of bringing medicines to cancer patients and other serious diseases. Director , Global Clinical Drug Supply will work in partnership with several… more
- Genmab (NJ)
- …(including clinical trial implementation, and oversight of all aspects of clinical development) working closely with the Medical Director and other ... of the clinical development plan (CDP) Author components with Medical Director and reviewer of clinical and regulatory documents and registration dossiers… more
- Genmab (NJ)
- …to the effective planning, and timely delivery of complete, high quality and reliable clinical trial data. The Associate Director DM will provide oversight to ... to the overall strategy, unified objectives and areas for development of Clinical OperationsEnsures data management activities and processes support the… more
- Merck & Co. (Rahway, NJ)
- …logistics support needs and/or Trade compliance consultation or operations support needsEnsure an exquisite partnership with Global Clinical Trial ... Job DescriptionThe Global Clinical Supply (GCS) organization, within our Research &...senior level stakeholders/GCS leadership and drive strategic decisions in support of GCS and the R&D portfolioStrong Ethics and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization, within our Research & Development (R&D) Division , is accountable for managing the 'end-to-end' ... integrated clinical supply chain across all of the R&D portfolio...senior level stakeholders/GCS leadership and drive strategic decisions in support of GCS and the R&D portfolioStrong Ethics and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Director , Clinical Development Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... Organization (CRO) Medical Monitor (MM):Provides oversight to the CRO MM for clinical data review activitiesMay support addressing eligibility and medical… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …lives for a living. Are you ready to make a difference? The Position The Director , Clinical Informatics in the Clinical Data Science & Evidence (CDSE) ... with research objectives Serving as an internal expert on clinical informatics tools development in support of...expert on clinical informatics tools development in support of organization-wide project and programs. Maintains knowledge of… more
- Insmed Incorporated (San Diego, CA)
- …for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Executive Medical Director of Ophthalmology, Clinical Development holds the responsibility ... to lead clinical programs across different diseases and supervise the clinical development team. This individual will be the primary point person for medical… more
- Merck & Co. (Rahway, NJ)
- …program cost estimates requested by Product Development Teams.- Responsible for authoring clinical supply documentation in support of labeling and packaging ... documentation to support critical Compound Management Coordination activities.- - Support the collection of clinical supply chain metrics and/or participate… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Regulatory Affairs and Clinical Safety Global Process Lead is responsible for overseeing and managing Global Regulatory Affairs & ... Clinical Safety global business processes. This includes defining and...collaboration is essential in developing and executing strategies that support the ongoing business needs of Global Regulatory Affairs… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … Clinical Data Science & Evidence (CDSE) department of NNI focused on clinical informatics tools development to support the CMR organization. This individual ... team in the (CDSE) department of NNI focused on clinical informatics tools development to support the CMR organization. This individual will serve as a… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …data (PED) evidence to support optimization of access & reimbursement, clinical practice, product development and registration. The Director serves as a ... ability in generating patient insights about disease and treatment to support clinical development, post-authorization, and commercial research activities across… more
- Merck & Co. (Rahway, NJ)
- …The applicant will preferably have experience with high concentration biologics to support clinical and commercial development. Maintaining a strong network ... & tri-specific antibodies, and fusion proteins as well as the biopharmaceutic support for the oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the… more
- Merck & Co. (North Wales, PA)
- …Director is aligned to: Scientific Exchange, Research, Scientific Congress Support , and Scientific Insights.Regional Medical Scientific Director 's liaise ... Job DescriptionRole SummaryThe Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in… more
- Merck & Co. (Rahway, NJ)
- …approach, driving the development of in vitro-in vivo relationships and preclinical-to- clinical translation in bioperformance of formulationsThe Director will ... & parenteral drug products for biologics as well as the biopharmaceutics support for the oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the… 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 ... FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved....study team, external service providers (CROs, vendors, etc.) and clinical sites to ensure all trial deliverables are met… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director of Regulatory Writing is a key role responsible for producing scientifically ... accurate, high-quality clinical regulatory documents while adhering to regulatory guidelines. This...strategic insights at the study team level. The Associate Director of Regulatory Writing must possess advanced knowledge of… 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 ... FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved....ready to make a difference? The Position The Senior Director of CMR Knowledge & Technical Advancement (KTA) Department… more
- Genmab (Plainsboro, NJ)
- …to be our best, and authentic is essential to fulfilling our purpose.The Role The Director of US Medical Affairs Solid Tumors Strategy will report to the Senior ... Director , US Medical Affairs Solid Tumors Strategy Lead. S/he...will provide medical affairs leadership for assigned asset(s)/indications and support for the overall oncology solid tumor portfolio. The… more
