• Clinical Study Mgr - 1

    Job Locations (All) | Mexico
    Posted Date 3 weeks ago(10/5/2018 12:50 PM)
  • Overview

    Organizes clinical studies and local teams for clinical research studies. Ensures studies are completed in accordance with study protocol, contract, and clients’ expectations. Serves as clinic contact for the study Sponsor and all internal groups.


    • Knowledge of GCP / ICH.
    • Demonstrated detailed knowledge of PRA SOPs, policies, and Work Instructions
    • Knowledge of pharmacokinetics and pharmacodynamics.
    • Read, write and speak English.
    • Qualified in Immediate Life Support.
    • Consult with project team members (with emphasis on the core team) and giving directions and instructions to Clinical Team Managers and staff at the clinic (effective influence plays an essential role).
    • Talk to, answer questions and inform representatives of sponsors and monitors.
    • Transferring knowledge and insights to employees.
    • Inform and guide volunteers in clinical trials
    • Inform and instruct subcontractors and making agreements with them.
    • Develop rules and instructions in English.
    • Conducting authorized medical procedures, as well as measurements, sampling, CPR, etc.


    • EDS-US: 1-3 years’ experience in a position with organizational/management duties were a major part of role.
    • EDS-NL: At least 1 year as Medical Research Associate (H.B.O. + (higher vocational) education level)
    • Bachelor’s degree or M.B.O. level (Secondary vocational education)
    • Specialization in a medical area. (EDS-NL)


    PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities.


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