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.
Information Notice:
The information on this page is intended for scientific, educational, and general informational purposes. Clinical approaches, availability, and regulatory status may vary by country, institution, and medical indication. For individual medical decisions, readers should consult qualified healthcare professionals and accredited medical centers.
The information on this page is intended for scientific, educational, and general informational purposes. Clinical approaches, availability, and regulatory status may vary by country, institution, and medical indication. For individual medical decisions, readers should consult qualified healthcare professionals and accredited medical centers.
Editorial Note:
This article has been prepared by the NBScience editorial team within the scope of clinical research, biotechnology, and international medical information.
This article has been prepared by the NBScience editorial team within the scope of clinical research, biotechnology, and international medical information.
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