• Clinical Research Physician

    Job Location(s) US-TX-Dallas
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  • Job Overview

    Clinical Research Physician

    Full Time

    Location: Dallas, TX


    Job Summary:

    Provides medical coverage for the Covance Clinical Research Unit. As Principal Investigator/SubInvestigator, responsible for assuring the health and welfare of participants. Responsible for performing medical procedures, responsible for proper conduct of the study trial, and responsible for all trial related medical decisions.


    • Duties and Responsibilities:


    • Responsible for protecting the rights, safety and welfare of participants under their care.
    • Responsible for ensuring that the clinical trial is conducted according to the investigational plan and all applicable regulations.
    • Provide medical and scientific feasibility of all new sponsor inquires.
    • Direct test article administration or dispensation.
    • Review and evaluate protocols and provide clinical and scientific support.
    • Liaise with sponsor regarding study design and site capabilities.
    • Interact with regulatory bodies as is relevant to clinical operations.
    • Attend study initiation meetings.
    • Present protocols at IRB/IEC meetings, as required.
    • Assist Operations and Client Managers with sponsor visits.
    • Perform pre-study physical examinations and review lab data to ensure volunteers are medically and mentally fit upon entering the study.
    • Perform on-study and post-study physical examinations to ensure that the physical and mental well being of volunteers is undiminished at the end of the study.
    • Inform Principal Investigator, IRB and Sponsor as appropriate of relevant events.
    • Review and sign CRFs at the conclusion of the study.
    • Delegate the above as appropriate.
    • Act as Principal Investigator/Co-Investigator as assigned by the Medical Director.





    • Active M.D or DO License
    • DEA License may be required


    • CPR/AED Certified




    Required: USA

    • 3-5 years MD experience

    Required: All sites

    • Experience in conducting clinical research preferred.



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