- Novo Nordisk Inc. (Stamford, CT)
- 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
- Merck & Co. (North Wales, PA)
- …and statistical analysis methods fundamental to effective pharmaceutical R&D.- The Clinical Safety Statistics (CSS) group within BARDS supports proactive assessment, ... Lead and provide statistical support for related drug/vaccine projects in Clinical Safety StatisticsInteract with Safety Physicians, Safety Scientists, Clinical … 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
- 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
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Associate Principal Scientist - Device Engineering and Early Development Lead ( Associate Director Equivalent)Our company's ... technical device development team(s) supporting individual drug assets currently in clinical development with line of sight to commercial filing and launch.… 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 ... SummaryThe Site Contracts and Budgets Management (SCBM) group, in Global Clinical Operations (GCO), develops strategy and provides oversight to all studies… 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)
- …existing and pipeline products to produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director, is a ... projects.Education:B.A. or BS degree, preferably in life sciences (ie, Medical Technology, Medical Laboratory Scientist, Clinical...to have a minimum of twelve (12) months of service in current position prior to applying for open… 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
- Merck & Co. (North Wales, PA)
- Job DescriptionRole SummaryThe Associate Director, Healthcare Quality Improvement is a role within the Global Professional Relations and Independent Medical ... with key external healthcare quality organizations and engagements with professional medical societies on ways to improve healthcare quality and guideline-concordant… more
- Merck & Co. (Rahway, NJ)
- …Laboratories ( drive break-through science through drug discovery, development and clinical evaluation to address significant unmet medical need.- Finance ... business.Under the guidance of the Director, Pharmaceutical Sciences and Clinical Supply (PSCS), this position is accountable for providing...to have a minimum of twelve (12) months of service in current position prior to applying for open… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …for the end-to-end delivery of External data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs ... and External Vendors for the data services they provide to support drug development processes and...and industry standard data collection practices preferred- 7+ years Clinical data management experience in a medical … 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
- 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)
- …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
- 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 II - Manufacturing Catalent Pharma Solutions in...line clearances in a Class 100,000 environment, maintenance of clinical trial material inventory logs;Duties include but not limited… 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
- 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. (Rahway, NJ)
- …their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs ... and risk management techniques to positively support and influence clinical and commercial combination product development and launches.Principal ResponsibilitiesLead… 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