- 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
- 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 complex studies… 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
- 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
- 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)
- …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
- 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
- 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
- Merck & Co. (Rahway, NJ)
- …activities include, but are not limited to:Reports to Executive Director or Associate Vice President, Therapeutic Area Lead .Develops worldwide product regulatory ... Job DescriptionOur Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Regulatory Affairs team bring new medical advancements to the world by facilitating communications and procedures that allow swift, organized ... of healthcare breakthroughs that help provide new, reliable, and compliant medical products, practices and solutions to the world.Looking for someone with… 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
- The Mount Sinai Health System (New York, NY)
- **JOB DESCRIPTION** ** Lead Medical Clinical Associate - IMA Nursing - MSH - FT M-TH 12:30PM-8:30PM, Fri 10AM-6PM, Alt. Sat 8AM-4PM** Through the ... performance of a variety of technical and routine tasks, the Lead Medical Clinical Associate contributes to patient care in an ambulatory setting, under… 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
- Fairleigh Dickinson University (Teaneck, NJ)
- Job Summary: Clinical Assistant/ Associate Professor & Clinical Director, Physician Assistant Program will develop, maintain, and ensure adequacy and quality ... lifespan. Working with the clinical coordinator, the Clinical Director will lead the development of...Director. This position, non-tenured and at the rank of clinical assistant or associate professor, serves as… more
- Hackensack Meridian Health (Hackensack, NJ)
- …mission to transform healthcare and serve as a leader ofpositive change. The Lead Clinical Research Nurse is responsible for providing guidance, training, and ... Administration. **Responsibilities** A day in the life of a Lead Clinical Research Nurse at Hackensack Meridian...Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified … 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
