- Merck & Co. (Rahway, NJ)
- Job DescriptionJob Overview:-We are seeking a highly qualified and experienced Associate Director in Data Management to lead our data management team in ... to drive data excellence and enhance the efficiency of our clinical research operations.Key Responsibilities:- Lead Data Management Initiatives:-Direct the… more
- Genmab (NJ)
- …our best, and authentic is essential to fulfilling our purpose.The Role:An Associate Director , Data Management is operationally responsible for the oversight of ... Clinical Data Management activities related to the effective planning, and timely...and timely delivery of complete, high quality and reliable clinical trial data. The Associate Director DM… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …around rare diseases and immune disorders. Summary This position works with the Director , Clinical Study Startup to establish the strategy driving global ... clinical study and post-marketing protocols and the Clinical Study Oversight Plan, day-to-day management of...where appropriate and escalate any complex problems to the Director , Clinical Study Startup.This position requires strong… more
- Genmab (Plainsboro, NJ)
- …is assigned to a trial the GCTM takes on the CTM role too.ResponsibilitiesLead the Clinical Trial Team (CTT) and Trial Management (TM) teamDefine and align CTT ... 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… 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
- Merck & Co. (Rahway, NJ)
- …of-Comparator Management ensuring timely planning, sourcing and management of Non-Company Commercial Products supporting clinical trials.Oversight ... Education:Bachelor's degree with 15+ years of professional experience that includes some clinical trial, supply chain-exposure or inventory management as well as… 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 ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people...of medical accountability and oversight for one or more clinical trials Matrix management responsibilities across the… 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...and retentionPerformance managementEnsure updated Business continuity plans and crisis management processes are ready at all timesOversight of our… more
- Merck & Co. (Rahway, NJ)
- …E2E product development process & connectivity between functions supporting pipeline (ie clinical development, Compound Management Coordination , supply chain, & ... Compound Management Coordination activities.- - Support the collection of clinical supply chain metrics and/or participate in critical non-pipeline activities as… more
- Insmed Incorporated (San Diego, CA)
- …for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Executive Medical Director of Ophthalmology, Clinical Development holds the responsibility ... experiencePreferred: A PhD in addition to the above10+ years of management experience in ophthalmology clinical development.Pediatric experience preferred.Gene… 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) ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...most diverse and collaborative groups within the organization. From health- care -provider interactions and developing and implementing regulatory strategies with… more
- Merck & Co. (Rahway, NJ)
- …as collaborative, and innovative culture in Global Regulatory Affairs and Clinical Safety for business process management and continuous improvement.-Establish ... accountability for processes execution throughout Global Regulatory Affairs and Clinical Safety through change management .-Develop, implement and report… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging ... trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs.… 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...you ready to make a difference? The Position Senior, Clinical Informatics leads the functions in the Clinical… more
- Merck & Co. (Rahway, NJ)
- …the Research & Development pipeline and realize its full potential. The Associate Director is expected to provide project management leadership and drive ... Project Manager is part of Global Project and Alliance Management (GPAM) which sits in the Research & Division...our company. - Position Description/Summary: - The GPAM Associate Director , Project Manager, is a core member of Early… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging ... immune disorders. Summary This position is responsible for providing project management , drug development expertise to Global Project Teams including strategic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Director , Development SOP Management Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of ... innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people...around rare diseases and immune disorders. Job Summary: The Director , Development SOP Management is responsible for… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Company is a global health care leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. Our Research ... portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …experience data (PED) evidence to support optimization of access & reimbursement, clinical practice, product development and registration. The Director serves as ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...most diverse and collaborative groups within the organization. From health- care -provider interactions and developing and implementing regulatory strategies with… more
