- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Device Development Associate Principal Scientist - Development Strategy, Design Controls and Risk Management Our company's ... and injection.This position will be responsible for leading and implementing medical device and combination product design controls and risk management activities… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our success is backed by ethical integrity, forward momentum, and ... Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team that will build biopharmaceutics… more
- Merck & Co. (Rahway, NJ)
- …robust scientific methodology we collaborate to discover and develop the next medical breakthrough. Our Company's success is backed by ethical integrity, forward ... Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team whose roles include design and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …will lead the execution and lifecycle management of Global Medical Affairs' externally sponsored clinical research (ESR) initiatives, ensuring strict ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...adherence to Good Clinical Practices (GCPs), relevant Standard Operating Procedures (SOPs), Food… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …of developing innovative cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo CAR-T cell therapy program. ... immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development team based… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … Safety and Pharmacovigilance, Regulatory/Risk Management, Quality Assurance, Medical Affairs, Translational Research, Research, Informatics Services, Project ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... those involving 3rd party development. This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for medium complexity… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... Statistical Analysis Plan (SAP), Statistical Analysis, Results Interpretation, and clinical study report (CSR): Leads statistical activities for complex studies… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and activitiesOversee the quality and timeline of vendor workCollaborate with study medical lead and biostat to ensure availability of necessary dataCoordinate ... and external stakeholder, co-development company, including authors, researchers, investigators, GMA medical leads, R&D clinical leads, bio stats and… more
- Eisai, Inc (Nutley, NJ)
- …evidence (RWE) development programs in support of global market access initiatives. Lead clinical meaningfulness initiatives that address issues such as payer ... At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides...company in Nutley, NJ. Assess real-world data gaps and lead evidence generation process for the collection and dissemination… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …directing the daily production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment. Job duties will be ... a team-based environment, on an assigned production shift schedule.Key Responsibilities Lead and supervise multiple units within the CAR-T process operations (ie… more
- AbbVie (Branchburg, NJ)
- …(IEST) lead , Clinical Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director, Clinical Development should ... @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Clinical Development will have global or regional… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …late phase development. The Associate Director reports to the Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide ... We are seeking an Associate Director to join out Oncology Clinical...day may include the following: + May function as lead Clinical Scientist for program, and/or as… more
- Bristol Myers Squibb (Madison, NJ)
- …activities as applicable + Evaluate innovative trial designs (collaboration with Medical Monitor/ Clinical Development Lead ) + Protocol and ... of assigned clinical trial activities. Serves as Clinical Trial Lead for one or more...reviewing, adjudication/resolution of cross functional comments and ensuring high clinical quality (collaboration with Medical Writing) +… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- Clinical Study Associate Manager (CSAM) role supports the Clinical Study Lead (CSL) by taking responsibility for areas of clinical trial delivery. ... Microsoft applications and TMF, as well as familiarity with medical terms, and a knowledge of Good Clinical... medical terms, and a knowledge of Good Clinical Practice and regulatory guidelines. Up to 25% travel… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …submission documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- J&J Family of Companies (New York, NY)
- ASSOCIATE CLINICAL ACCOUNT SPECIALIST INTERN (Summer 2025) - New York, NY - Johnson and Johnson - 2406207612W **Description** Johnson & Johnson - Med Tech - ... Electrophysiology is recruiting for ** Associate Clinical Account Specialist (ACAS) Intern (Summer...and treating heart rhythm disorders. J&J is the #1 medical device company in electrophysiology (EP) and the first… more
- J&J Family of Companies (Raritan, NJ)
- Associate Director, North America Regulatory Lead - 2406196976W **Description** Johnson & Johnson Innovative Medicine is recruiting for Associate Director, ... reach their potential. At Johnson & Johnson, we all belong. The Associate Director, Regulatory Affairs will be responsible for the development, implementation, and… more
