• Team Lead East - Senior Director, US…

    Merck (Columbus, OH)
    **Job Description** **Role Summary** + The Regional Medical Scientific Senior Director Team Lead (RMSD TL) is a credentialed therapeutic and disease expert (MD, PhD, ... our company's performance principles through routine field observation/coaching visits, internal and external stakeholder feedback and field/customer metric analysis.… more
    Merck (11/20/25)
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  • Senior Precision Medicine Associate- FSP

    Parexel (Columbus, OH)
    Parexel FSP has an exciting opportunity for a Senior Precision Medicine Associate. This role works closely with line Manager, Precision Medicine, and other key ... + Collaborates within cross functional study teams + Presents at investigator meetings and creates training materials (lab manual, sample collection procedures… more
    Parexel (11/08/25)
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  • Senior Cyber Incident Responder

    Highmark Health (Columbus, OH)
    …and aid in formulation and execution of security strategy for the team. The Senior Cyber Incident Responder interfaces with other internal teams to determine ... **Company :** enGen **Job Description :** **JOB SUMMARY** This Position is the top investigator in the Cyber Fusion Center, capable of working any kind of incident,… more
    Highmark Health (10/16/25)
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  • Clinical Research Associate II/Sr. Clinical…

    Parexel (Columbus, OH)
    …candidates based in the Midwest, West Coast, Northeast & North Carolina The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site ... monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study...in Oncology) + Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases + Must be fluent… more
    Parexel (11/22/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Columbus, OH)
    …with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study teams on TA indication and ... trials for local sponsorship as needed with the support of the designated Senior Medical Director/ Global Head of TA (as appropriate) Pharmacovigilance Support *… more
    Parexel (10/11/25)
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  • Associate Director, Regulatory Affairs

    Sumitomo Pharma (Columbus, OH)
    …CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed ... Ensure compliance with global regulatory requirements and adherence to regulatory internal policies and processes and coordinate regulatory compliance activities at… more
    Sumitomo Pharma (11/20/25)
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  • Associate Director, Regulatory Affairs (Oncology)

    Sumitomo Pharma (Columbus, OH)
    …Ensure compliance with global regulatory requirements and adherence to regulatory internal policies and processes and coordinate regulatory compliance activities at ... CMC documentation (eg nonclinical study reports, clinical protocols/study reports, investigator brochures, CMC information/data) and contributes to content as needed… more
    Sumitomo Pharma (10/11/25)
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  • Research Scientist-Health Services Research

    Elevance Health (Mason, OH)
    …and presents key study insights to the champions, including Elevance Health senior leadership team, internal decision makers, and other external ... research project proposal development from early conceptual stages for external and internal submissions. + Provides scientific rigorous input in the design and… more
    Elevance Health (11/24/25)
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  • Sr. Research Data Technology Consultant - REDCap,…

    OhioHealth (Columbus, OH)
    …in our careers and in our communities. **Job Description Summary:** The Senior Consultant, Research Data and Technology, will develop and lead specialized technical ... leader of multidisciplinary teams establishing and maintaining communications with Investigator , project teams, sponsor, and others. **Responsibilities And Duties:**… more
    OhioHealth (10/01/25)
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  • Manager, Clinical Trials

    Bausch + Lomb (Columbus, OH)
    …protocol development, case report form (CRF) development, IRB submissions, investigator agreements, informed consent form (ICF) development, site selection and ... communication with senior clinical trial sites regarding all logistics including contract...Trial Materials, Marketing, Regulatory, and Quality/Compliance. + Liaising between internal and external stakeholders to facilitate cooperation of others.… more
    Bausch + Lomb (11/19/25)
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