- 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 ... trials, some of more recent years working as an employee in clinical , medical and/or regulatory in the pharmaceutical, biotechnology, CRO, and/or healthcare… more
- Novo Nordisk Inc. (Phoenix, AZ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Eisai, Inc (NJ)
- …activities related to the outsourcing of clinical services to Clinical Research Organizations (CROs) and functional service providers for Eisai's R&D ... make a difference. If this is your profile, we want to hear from you. Job Summary The Associate Director, Clinical Outsourcing, will oversee and lead and support… more
- Merck & Co. (North Wales, PA)
- … clinical protocol(s).Serves as the lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on clinical /scientific and ... medical monitoring team in review and interpretation of clinical data/ medical protocol-deviations in collaboration with the...to have a minimum of twelve (12) months of service in current position prior to applying for open… more
- Merck & Co. (Rahway, NJ)
- …to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human ... uses big data to analyze the safety and efficacy claims of our potential medical breakthroughs. We review the quality and reliability of clinical studies using… more
- Merck & Co. (North Wales, PA)
- …includes, but is not limited to: Reporting to Senior Management of the Medical Device and Combination Product (MDCP) Quality Assurance Operations team, the ... Associate Director Quality Engineering & Quality Assurance is responsible...Quality Assurance is responsible for independent compliance support of Medical Devices including the device constituent part of Combination… more
- Merck & Co. (North Wales, PA)
- …to train internal stakeholders, including Field Sales representatives, Our Company National Service Center (call center), country medical colleagues, and United ... IS A HYBRID ROLE. AN ONSITE PRESENCE IS REQUIRED The Global Medical Information (GMI) Scientists for Oncology, with their advanced scientific background (PharmD,… more
- Merck & Co. (North Wales, PA)
- …and robust scientific methodology we collaborate to discover the next medical breakthrough.Position Description: The Associate Principal Scientist Statistical ... to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …treatment of multiple myeloma. Legend Biotech is seeking a CAR-T Warehouse Operations Associate as part of the Technical Operations team based in Piscataway, NJ. The ... CAR-T Warehouse Operations Associate will be part of the Technical Operations team...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… 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 ... Clinical Ancillary Management project teams to ensure Clinical Ancillary Management services are defined and...those most recent years working as an employee in clinical , medical and/or regulatory in the pharmaceutical… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionBiologics Process R&D Associate ScientistOur Research Scientists are our Inventors.- Using innovative thinking, state-of-the-art facilities, and ... robust scientific methodology, we partner to deliver the next medical breakthrough.Biologics Process Research & Development (BPR&D) within our company's Research… 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 ... and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product… more
- Catalent (San Diego, CA)
- …formulation development, GMP manufacturing and stability storage and testing as well as Clinical Supply Services . At Catalent San Diego, we recruit and develop ... Quality Assurance Associate I, ManufacturingCatalent Pharma Solutions in San Diego...production audits in a Class 100,000 environment, maintenance of clinical trial material inventory logs.Other duties as assignedThe Candidate:… more
- Merck & Co. (Rahway, NJ)
- …reliance on automation within Biologics Process Research & Development (BPR&D).The Associate Director role-will provide process automation leadership within the BDC ... automation activities throughout the facility.-Primary Responsibilities:Provide process support for clinical manufacturing and R&D processes while also facilitating tech… more
- Insmed Incorporated (Bridgewater, NJ)
- …(FDA, EMA, PMDA)Manage customized bioanalytical assays via network of external service providers in advance of and during clinical development.Participate ... for Millennials™ lists.OverviewWithin the Translational Bioanalytical Sciences (TBS) group of Clinical Development, the role focuses on LC-MS/MS of small and large… more
- Merck & Co. (Rahway, NJ)
- …in and/or leads cross-divisional technical teams focusing on late-stage clinical process development, characterization, and/or technology transfer and validation ... and inventiveness to help make meaningful contributions to global medical advancement. At Our Company, we're inventing for life.NOTICE...to have a minimum of twelve (12) months of service in current position prior to applying for open… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development team based ... 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. If you're… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical Development, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within ... of clinical trials is required Demonstrates technical expertise within Clinical Development, Medical Affairs, and Regulatory Affairs (CMR), staying… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... of sourcing strategies for a specific set of R&D categories (CRO, Medical Writing, BDM, etc..). Builds strategic plans for specific categories under the… more
- Merck & Co. (North Wales, PA)
- …talented and dedicated colleagues while developing and expanding your career.The Clinical Director (Principal Scientist) has primary responsibility for the planning ... and directing clinical research activities involving new Oncology medicines within an...the Director may be responsible for: Providing scientific and medical leadership for strategic alliances and Co-partnership opportunities.-Supporting the… more
