Physician / Clinical Research / Florida / Locum or Permanent / Principal Investigator Job

Duties & Responsibilities: Evaluate patient eligibility for a clinical trial as per protocol. Review and discuss study protocols and obtain (or delegate) informed consents from with patients during designated study visits to perform assessments, including physical examinations and data collection. Review and interpret laboratory results, EKGs and other diagnostic and safety assessments as required per study protocol. Monitor all safety variables, including adverse events, laboratory abnormalities, changes in patient medical status, evaluation of prescribed concomitant medications as per protocol, and un-blinding requests. Use proper medical judgment in the interpretation and decision-making as it relates to the investigational study. Review, approve and ensure timely reporting of eCRFs, protocol deviations and Serious Adverse Events (SAE).Ensure accurate documentation of study-related procedures. Ensure proper use and storage of Investigational Product. Ensure prompt reporting all unanticipated problems or injuries to IRB, Sponsor, or delegated with FDA, IRB, Sponsors, CROs, or their delegated representatives as needed throughout the study. Review and discuss any medical or protocol-related concerns with medical monitors. Attend Investigator Meetings and other study-related meetings. Review and approve Clinical Study Agreements. Work with Sub-investigator(s), Clinical Research Coordinators, and key study personnel in overseeing the execution of study protocols.