- Merck & Co. (Rahway, NJ)
- …of statisticians and the statistical programmers to ensure that all programs meet analysis requirements, internal standard operating procedures, and external ... innovative statistical methods and applications in clinical trial development. Education and Minimum Requirement: PhD or equivalent degree in… more
- Tris Pharma (Monmouth Junction, NJ)
- …Monmouth Junction, New Jersey, Tris has an immediate opening for a full-time permanent Director / Senior Director , Clinical Quality Assurance. This is a hybrid ... Title commensurate with experience.SUMMARY:Reporting to the Chief Quality Officer the Senior Director of Clinical Quality Assurance provides strategic leadership… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an ... events based upon approved Safety Management Team (SMT) materials- Supports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an ... events based upon approved Safety Management Team (SMT) materialsSupports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety… more
- Merck & Co. (Rahway, NJ)
- …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... compliance mindset and collaboration with various partners and stakeholders in development.The Director will report to the Executive Director of Biologics and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …processes, and on Joint Alliances. Assess and articulate regional interdependencies, program regulatory risks, and opportunities in the development of global ... regulatory precedence and competitive landscape with respect to impact on development programs . Ability to serve and participate on internal and external panels… more
- Merck & Co. (Millsboro, DE)
- …regulatory inspections (USDA, DEA, DNREC, etc.) of animal facilities and program reviews is required.PurposeThe Associate Director /Attending Veterinarian will ... Job DescriptionAssociate Director , Animal ServicesAbout the JobAnimal Health in Millsboro...well as for the veterinary care and animal husbandry program at our company's Millsboro Animal Health facilities. This… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …position will define and oversee the translational strategy/plan for oncology therapeutic program /s in global R&D. The successful candidate will set goals and ... Lead, Non-Clinical Research, Medical Affairs and other stakeholders to support the program . Other responsibilities will include, but not be limited to, identifying… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for regulatory CMC (Chemistry, ... that facilitates Health Authority reviews.- Supports company`s GMP Change Management Program . Evaluates CMC changes for portfolio biologics and determines filing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of Clinical Development processes. Job Description:Execute an overarching safety program tailored for AEs from end-to-end: understanding predisposing non-clinical ... limited to protocol amendments, Dear HCP letters and key medical education initiatives.Develops prospective contingency plans for management of assigned safety risks… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary The Associate Director , Program Management is a senior position responsible for ... functions in Daiichi Sankyo (DS). Reporting to the Sr. Director , Enterprise Program Management, this position requires...the coordinated delivery of all projects contained in the programs they manage. Program level responsibilities start… more
- Merck & Co. (North Wales, PA)
- Job DescriptionUnder the guidance of a Senior Director , within Outcomes Research (OR) the incumbent has the following responsibilities: Development of the ... Teams, Regional Product Directors, our company's affiliates, Public Affairs, and Medical Education to ensure value evidence programs are consistent with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …executing national advisory boards, assists with defining strategies to support medical education programs and reviews IME grant proposals, represents Medical ... Key Opinion Leaders (KOLs), Healthcare Professionals (HCPs), and other stakeholders. The Medical Director will also assist the Senior Medical Director in… more
- Merck & Co. (Rahway, NJ)
- …responsible for building and executing CMC development plans.Under the guidance of the Director & Portfolio Lead, the core responsibility of this individual will be ... line of sight across the development lifecycle and maintaining programs in harmony with the portfolio. In addition, the... in harmony with the portfolio. In addition, the Senior Specialist will be expected to participate in development… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Director Global Medical Affairs Oncology (GMA), ADC, under the direction of the Senior Director , GMA Oncology ADC (Global Medical Affairs team lead for ... compound), is responsible for assisting with defining compound/ program medical strategies and for leading select medical affairs...and other scientific exchange activities in alignment with the Senior Director , such as scientific symposium and… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionThe Director of Immuno-Metabolism will be responsible for overseeing and facilitating the research in metabolic disorders & inflammation, in the ... diseases and build a robust pipeline of drug discovery programs .Serve as a core member of the Discovery CMD...delivers on target identification & validation and advances CMD pipeline. Education Requirement: PhD, MD, or MD/PhD degree in Metabolism… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program . This Clinical Science (CS) Group Lead ... will be responsible for overseeing multiple program -level CS Asset Leads who are managing a team...throughout the project life cycle is optimized across multiple programs . The CS group lead will also contribute to… more
- Merck & Co. (Rahway, NJ)
- …oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team ... portfolio and influence bridging strategies across the portfolio. The Biopharmaceutics Director will work with their direct reports to proactively develop and… more
- Merck & Co. (North Wales, PA)
- …company's innovations and improve patient health outcomes. Under the guidance of a senior leader, this individual will serve as an Oncology, V&I, Outcomes Research ... lead for a Lung Cancer program . Primary Responsibilities: Lead in value evidence teams in...value evidence strategies for in-line and pipeline products. Obtain senior management approval of value evidence generation plans. Provide… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for developing and continually growing strong relationships with DS internal senior stakeholders to assess, develop, implement and drive execution of Strategic ... for given commodities/business areas and leading the overall supplier relationship management program for DSI, for DS products and alliances. Cultivates a high… more
