• Merck & Co. (Rahway, NJ)
    …This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in review and interpretation of ... the scientific planning and execution of one or more clinical trials or significant aspects thereof. -In this position,...of twelve (12) months of service in current position prior to applying for open positions.If you have been… more
    HireLifeScience (03/26/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials ... Essential functions include, but are not limited to:Performs primary medical review -of serious adverse experience reports and other AE reports of interest… more
    HireLifeScience (03/23/24)
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  • Merck & Co. (North Wales, PA)
    …study start up (eg, database set up)Lead medical monitoring team in review and interpretation of clinical data/medical protocol-deviations in collaboration with ... drives scientific planning, strategy and execution of Phase 1-4 clinical studies.-Under the direction of the Program Lead, you...of twelve (12) months of service in current position prior to applying for open positions.If you have been… more
    HireLifeScience (03/22/24)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …& retention activities Obtain expert medical community input Regulatory liaison: Write and/or review clinical sections of clinical trial reports, statistical ... certification or relevant therapeutic area experience in diabetes, CV or Obesity required Prior clinical research or related experience (eg monitoring of … more
    HireLifeScience (03/15/24)
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  • Novo Nordisk Inc. (Tucson, AZ)
    …guidelines, chronic care models, protocols, etc. to engage HCPs in clinical conversations to appreciate how they manage patients with diabetes and where they ... the opportunity to help people with obesity receive the care they deserve. The Novo Nordisk aspiration is to...maintain advocacy of customers aligned to company, brand and clinical goals. The OCS develops local strategies and executes… more
    HireLifeScience (03/27/24)
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  • Novo Nordisk Inc. (Boston, MA)
    …guidelines, chronic care models, protocols, etc. to engage HCPs in clinical conversations to appreciate how they manage patients with diabetes and where they ... About the Department The Cardiometabolic Care Sales Team is at the forefront of...Representative also assists their target physicians with their local clinical and educational initiatives by coordinating company resources (eg,… more
    HireLifeScience (03/28/24)
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  • Merck & Co. (North Wales, PA)
    …9 years Statistical Analysis System (SAS) programming experience in a clinical trial environment.MS (preferred) in Computer Science, Statistics, Applied Mathematics, ... years Statistical Analysis System (SAS) programming experience in a clinical trial environment.Required-Experience and Skills:Expertise in SAS for system development… more
    HireLifeScience (03/27/24)
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  • George Washington University (Washington, DC)
    …teams; Oversees the administrative, regulatory, and programmatic activities of the Institutional Review Boards (IRB); Institutional Animal Care and Use Committee ... supporting the university's Human Research Protection Program (HRPP), animal care and use program, and oversight committees for the...on GW's Federal Wide Assurance (FWA); Ensures a thorough review of research protocols prior to submission… more
    JobGet (03/11/24)
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  • Novo Nordisk Inc. (Chicago, IL)
    About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health- care -provider interactions and developing and implementing regulatory strategies with...the SD serves as a key member of the Clinical Trial Strategy Team, provides additional analytic support to… more
    HireLifeScience (03/20/24)
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  • Novo Nordisk Inc. (Olive Branch, MS)
    …who need them most. At Novo Nordisk, we are the world leader in diabetes care and a major player in defeating other serious chronic conditions such as obesity, ... in order to influence formulary status, as applicable May analyze impact of managed care in the territory and its effect on prescribing decisions, and modify sales… more
    HireLifeScience (03/28/24)
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  • Merck & Co. (North Wales, PA)
    …to the Director/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and ... objectives.Serve as the liaison and manages correspondence with FDA's promotional review divisions Office of Promotion and Advertising Review (OPDP)/Advertising… more
    HireLifeScience (03/01/24)
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  • Merck & Co. (Rahway, NJ)
    …and late-stage clinical development to execute on biomarker strategies in clinical trials. Write and review validation and bioanalytical assay final reports, ... Molecular Biomarkers (TMB) is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of … more
    HireLifeScience (03/27/24)
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  • Merck & Co. (Rahway, NJ)
    …and late-stage clinical development to execute on biomarker strategies in clinical trials.Write and review validation and bioanalytical assay final reports, ... Molecular Biomarkers (TMB) is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of … more
    HireLifeScience (03/27/24)
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  • Merck & Co. (Rahway, NJ)
    …company's clinical supply programs. This person will also independently review and approve documentation accompanying the disposition of API materials (including ... to API (including new modalities) manufacturing in a complex, clinical supply development. - Review and/or approve...of twelve (12) months of service in current position prior to applying for open positions. - If you… more
    HireLifeScience (03/23/24)
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  • Merck & Co. (Rahway, NJ)
    …supply API manufacture, testing, release and maintenance in support of our company's clinical supply programs. This person will also review and approve ... to API (including new modalities) manufacturing in a complex, clinical supply development.- Review and/or approve GMP...of twelve (12) months of service in current position prior to applying for open positions. - If you… more
    HireLifeScience (03/23/24)
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  • Novo Nordisk Inc. (New York, NY)
    care for the "at risk" diabetes patient population (Eg, providers, care coordinators, quality, population health, clinical pharmacy) Educate providers on ... Novo Nordisk, we are the world leader in diabetes care and a major player in defeating other serious...exceeding the Novo Nordisk points threshold assigned based on review of Motor Vehicle Records. Qualifications A Bachelor's or… more
    HireLifeScience (03/26/24)
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  • Merck & Co. (Rahway, NJ)
    …enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training ... for and support batch processing readiness and execution activities.Prepare, review , and/or approve GMP Documentation as appropriate.Author/Approve Standard Operating… more
    HireLifeScience (03/26/24)
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  • Merck & Co. (North Wales, PA)
    …and Label Evaluation and Development Team.Conducts initial Investigational New Drug application/ Clinical Services Agreement content review and approval to ... and/or subsidiaries for all applications and submissions. Responsible for regulatory review and final approval for all submissions and associated documentation.… more
    HireLifeScience (03/01/24)
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  • Merck & Co. (KY)
    Job DescriptionThe Vaccine Customer Representative (VCR) supports customers by providing clinical information on our Company's vaccines, as well as education and ... variety of customers within their assigned geography.- These customers may include health care pro viders such as physicians, nurses, pharmacists as well as quality… more
    HireLifeScience (03/27/24)
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  • Merck & Co. (Rahway, NJ)
    …approaches to develop and implement translational PK/PD strategies, characterize clinical pharmacokinetics and pharmacodynamics of new chemical entities and ... models, quantitative system pharmacology (QSP) and disease progression models, clinical trial design via outcome/enrollment modeling and simulation, comparator… more
    HireLifeScience (03/05/24)
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