Position Summary

Ensures adherence to protocol requirements, protecting the rights and welfare of study subjects, assuring the integrity of data generated at the site. In executing these position responsibilities, the Investigator is guided by and promotes adherence to FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Essential Job Functions

  • Employee Mentoring
  • Protocol Planning and Oversight
  • Investigator Qualifications and Agreements
  • Ensure Protocol Compliance
  • Ensure Adequate Review by A Duly Constituted Institutional Review Board (IRB)
  • Manage the Care of Subjects
  • Protect the Rights and Welfare of Subjects
  • Ensure Validity of The Data Reported to The Sponsor
  • Ensure Documentation of Study-Related Procedures, Processes and Events
  • Ensure the Proper Use and Storage Of Investigational Agents
  • Study Communication
  • Business Development
  • Maintains Professional and Technical Knowledge

M.D, D.O., or PhD required

Learn more about being a provider at RCR here.