- 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. (WA)
- 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)
- …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
- 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. (North Wales, PA)
- Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central source of information regarding publication activities and is responsible for ... and implementation of global publication strategies and tactical plans. The Associate Director Pub Manager oversees compliance with our company's publication… 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
- 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. (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
- 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
- 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
- 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
- The University of Vermont Health Network (Burlington, VT)
- …upon completion of one year of satisfactory service in the same department.The Clinical Care Associate (mirrors the Medical Assistant role in the ... for our patients, families and the practices within a medical home. The incumbent is involved in direct patient...care under the direction of a provider and performs clinical and administrative health care support services … 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)
- …oversight of, contractors performing various GMP activities supporting the production of clinical supplies with focus on drug product. Additionally, experience in ... medical device and/or combination products would be preferred.- Key...to have a minimum of twelve (12) months of service in current position prior to applying for open… 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
- 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 ... and is accountable for the development and control of Clinical Project Budget in support of Phase I-III ...motivate and develop staff to ensure high degree of service is maintained and staff remains focused on corporate… 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …up Must have solid understanding of the pharmaceutical marketplace including legal, medical , regulatory and clinical processes Develops accurate short- and ... brand marketing, market access, commercial insights and analytics, sales, medical /CMR, legal, compliance, and regulatory. Other internal relationships include Public… more