• Clinical Research Specialist

    Beth Israel Lahey Health (Burlington, MA)
    …Research Associate Submits DR-1, study protocol, study consent form, Investigator's Brochure, IDI , IDE, CVs and Medical Licenses and all associated articles of ... information to the IRB in a timely manner. Submits all protocol amendments / consent form revisions, adverse events, notification of change in risk to the IRB in a timely manner. Attends Investigator's Meetings. Reviews study content for potential… more
    Beth Israel Lahey Health (05/01/24)
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