Screens potential participants, explains study details, obtains informed consent, schedules visits, and acts as a primary contact for subjects.
Organizes study files, prepares and submits regulatory documents (like IRB submissions), manages study budgets, and maintains trial-specific logs.
Ensures the trial follows the specific scientific protocol, protecting data integrity and participant safety.
Collects, organizes, and manages research data, including case reports and drug accountability records, often working with data management teams.
Trains research staff, arranges study equipment, and communicates with laboratories and
Upholds ethical standards, ensuring patient rights and well-being are prioritized throughout the study.