Responsibilities
Liaison between sponsors, investigators and coordinators.
Ability to recruit studies.
Completion of IRB documents.
QA of source documents.
Contract and budget review.
Requirements
Requires knowledge of clinical trials, regulatory requirements, GCP and study coordinator supervision. Must have substantial trial experience.
Interested in learning whether current clinical programs, research developments, or emerging therapeutic approaches may be relevant to your situation?
Educational and research information only. Individual medical decisions should be made in consultation with qualified healthcare professionals.
0 Comments