• Merck & Co. (Rahway, NJ)
    …Description: This role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the Clinical Research Director (CRD) ... person is responsible to manage a team of 6-14 Clinical Research Associates (CRAs) and to ensure excellent study...more detail, please contact your HRBP or Talent Acquisition Advisor . Employees working in roles that the Company determines… more
    HireLifeScience (05/11/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials ... to produce safe, effective, innovative medicine.The position manages all aspects of clinical trial operations in a country and will manage exquisite execution of… more
    HireLifeScience (05/10/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Global Clinical Data Standards Therapeutic Area Lead The Associate Director, Global Clinical Data Standards Therapeutic Area ... expert in the area of data standards as it relates to developing clinical data collection tools. The individual may be responsible for coordinating data processes… more
    HireLifeScience (05/10/24)
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  • Merck & Co. (North Wales, PA)
    …Summary: This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the ... cross-functional team.Job Responsibilities: Responsible for leading specific aspects of clinical /scientific execution of clinical protocol(s). This may… more
    HireLifeScience (05/09/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionOur Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... new indications for existing products. We ensure we conduct high-quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific… more
    HireLifeScience (05/08/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionThe Clinical Pathology Scientist (Principal Scientist) supports clinical teams in the use of pathology in clinical trials, ensuring timelines ... of our development programs. This position will work closely with the Head of Clinical Imaging and Pathology, Pathology Leads, and other Clinical Pathology and… more
    HireLifeScience (05/07/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionPosition Description: Manager, Operations and Reference Data Management, Global Clinical Data Standards Working closely with the Global Clinical ... efficiency, and productivity across the organization. Keeps abreast of project management, clinical data standards, and regulatory requirements for clinical data… more
    HireLifeScience (05/08/24)
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  • Merck & Co. (North Wales, PA)
    …SummaryThis position contributes to the scientific planning and execution of one or more clinical trials in the lung cancer program. Assists the Lead Clinical ... Scientist and study team with the scientific conduct of clinical studies. In this position, you will have the opportunity to develop your leadership, technical… more
    HireLifeScience (05/04/24)
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  • Merck & Co. (Rahway, NJ)
    …new medicines to patients. The key areas of focus include: (1) diversity in clinical trials, (2) clinical trial recruitment and (3) general education and ... awareness of clinical trials. This job is the ultimate reminder that...more detail, please contact your HRBP or Talent Acquisition Advisor . Employees working in roles that the Company determines… more
    HireLifeScience (05/04/24)
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  • Merck & Co. (Rahway, NJ)
    …(Principal Scientist)has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our ... company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of clinical more
    HireLifeScience (05/04/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionAs a key member of the General Medicine Global Clinical Development team, the Vice President/ Therapeutic Area (TA) Head's primary objectives will be ... Development Teams (PDTs) and collaborating with Section Heads, PDT Leaders, and Clinical Directors responsible for the design and medical monitoring of clinical more
    HireLifeScience (05/02/24)
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  • 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
    HireLifeScience (05/04/24)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionOur Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials ... and pipeline products to produce safe, effective, innovative medicine.The Global Clinical Data Standards Vocabulary Specialist, Associate Director, is a subject… more
    HireLifeScience (04/19/24)
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  • Merck & Co. (Rahway, NJ)
    …Laboratories ( drive break-through science through drug discovery, development and clinical evaluation to address significant unmet medical need.- Finance is a ... business.Under the guidance of the Director, Pharmaceutical Sciences and Clinical Supply (PSCS), this position is accountable for providing comprehensive… more
    HireLifeScience (05/09/24)
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  • Merck & Co. (Rahway, NJ)
    …Molecular Biomarkers (TMB) is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of ... clinical development at our company's Research laboratories. TMB laboratories...more detail, please contact your HRBP or Talent Acquisition Advisor .#EligibleforERPEmployees working in roles that the Company determines require… more
    HireLifeScience (05/11/24)
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  • Merck & Co. (North Wales, PA)
    …is responsible for developing medical writing deliverables that support the clinical regulatory writing portfolio. With minimal oversight, the Senior Medical ... Writer:Demonstrates independence in preparing clinical regulatory documents (eg, protocols, clinical study reports, investigator's brochures, clinical more
    HireLifeScience (05/09/24)
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  • Merck & Co. (North Wales, PA)
    …a key collaborator with internal and external stakeholders including Statistics, Clinical Research, Regulatory, Observational Research, Clinical Safety and PK/PD ... operational challenges that require strategic solutions, resulting in improved Clinical Study Report and filing completion timelines worldwide.Lead development of… more
    HireLifeScience (05/10/24)
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  • Merck & Co. (North Wales, PA)
    …knowledge and editorial skills to contribute to medical education and clinical decision support for healthcare professionals, while also providing high quality ... viewed by more than 1 billion users each year.A minimum of 5 years clinical experience and demonstrated writing skills are mandatory. Current clinical activity… more
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  • Merck & Co. (Rahway, NJ)
    …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed Oncology medicines. Our ... company's Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Director will manage the entire cycle of clinical more
    HireLifeScience (05/04/24)
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  • Merck & Co. (Rahway, NJ)
    …in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects related to ... clinical pharmacology and pharmacometrics of oncology drugs from post-PCC...more detail, please contact your HRBP or Talent Acquisition Advisor .Employees working in roles that the Company determines require… more
    HireLifeScience (05/10/24)
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