Job Description

• 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.

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