• Merck & Co. (North Wales, PA)
    …Description: Essential functions include, but are not limited to:Performs primary medical review-of serious adverse experience reports and other AE reports of ... to safety inquiries from health care professionals, regulatory agencies, subsidiary staff and other internal customers in conjunction with the CSRM… more
    HireLifeScience (03/23/24)
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  • 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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the… more
    HireLifeScience (02/01/24)
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  • Novo Nordisk Inc. (Dallas, TX)
    …live with the disease of obesity, yet only 2% of them receive dedicated medical treatment. By joining the Obesity Commercial team, you will have the opportunity to ... on customer engagements and execution of our strategy. As one of the Novo Nordisk must win battles, developing...relevant local stakeholders, to empower proactive, systematic, and chronic medical management of Obesity and foster relevant use of… more
    HireLifeScience (03/28/24)
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  • 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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the… more
    HireLifeScience (03/28/24)
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  • 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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the… more
    HireLifeScience (03/28/24)
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  • 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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the… more
    HireLifeScience (03/27/24)
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  • 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 ... stage drug/vaccine clinical development projects. This may include leadership of one or more projects. Accountability predominantly includes the development and… more
    HireLifeScience (03/26/24)
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  • 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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the… more
    HireLifeScience (03/28/24)
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  • 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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the… more
    HireLifeScience (03/26/24)
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  • Novo Nordisk Inc. (Los Angeles, CA)
    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 implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and...efficacy and new product development, CMR is involved. The one thing that keeps us all marching to the… more
    HireLifeScience (03/22/24)
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  • Merck & Co. (North Wales, PA)
    …to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human ... programming deliverables through the use of global outsource partner programming staff .Develop and manage project plan using Microsoft Project or similar… more
    HireLifeScience (03/27/24)
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  • Merck & Co. (North Wales, PA)
    …results of safety evaluations to the project teamsMentor and guide junior staff in functional activities.Skills Education and Minimum Requirement: PhD or equivalent ... and execution. Preferred Skills and Experience :Publications in peer reviewed statistical/ medical journals.-An understanding of biology of disease and drug discovery… more
    HireLifeScience (03/27/24)
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  • Merck & Co. (Rahway, NJ)
    …- Ability to work across functional and sites, with all levels of staff and management. - Qualified candidates should have proficiency with Microsoft Suite (Word, ... Skills: - Experience in the pharmaceutical , biotechnology, chemical, medical device, or closely related industry. - Experience in... device, or closely related industry. - Experience in one or more functional areas such as quality assurance,… more
    HireLifeScience (03/23/24)
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  • Merck & Co. (Rahway, NJ)
    …chemical, medical device, or closely related industry.- Experience in one or more functional areas such as quality assurance, laboratory, manufacturing, ... Ability to work across functional and sites, with all levels of staff and management.- Qualified candidates should have proficiency with Microsoft Suite (Word,… more
    HireLifeScience (03/23/24)
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  • Daiichi Sankyo, Inc. (Munich, ND)
    …in a medical environment preferred.Familiarity to a Japan-based organization preferred. Travel Ability: to travel up to 30% In-house office position that ... to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class...internally to OEDC leadership, including the OEDC Chief of Staff (COS) in establishing and facilitating an effective world… more
    HireLifeScience (02/02/24)
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  • 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 ... Development Center (OEDC) so as to be regarded as one of the world's most innovative, trustworthy, and experienced...This position provides direct oversight of the internal OEDC staff necessary for meeting the daily operations as well… more
    HireLifeScience (01/10/24)
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  • Merck & Co. (North Wales, PA)
    …to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human ... with clinical pharmacology concepts and pharmacokinetics concepts.Experience with at least one other software than SAS (eg, R, NonMem).Good working knowledge of… more
    HireLifeScience (02/24/24)
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  • Merck & Co. (Rahway, NJ)
    …and manages a small team of information scientists and vendor staff .-Leads all aspects of the screening, indexing, abstracting, literature acquisition, and ... monitoring requirementsMaintains expertise in developments in the fields of medical information, regulatory policy, adverse event reporting,Identifies and utilize… more
    HireLifeScience (03/22/24)
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  • Merck & Co. (Rahway, NJ)
    …monitors, coordinates, and evaluates the work of vendor screening/abstracting/indexing staff to ensure effective and efficient collection, storage, and dissemination ... functions Maintains personal awareness of developments in the fields of medical information, regulatory policy, adverse event reporting, information storage and… more
    HireLifeScience (03/22/24)
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  • Insmed Incorporated (San Diego, CA)
    …leadership and management of a clinical study(s) and clinical operations aspects of one or more drug development program(s) in compliance with GCP and relevant ... vendor selection and review contracts/work orders.Provide mentorship to assigned study staff (CTMs, CTAs) or colleaguesReview metrics and Key Performance Indicators… more
    HireLifeScience (03/12/24)
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