Job Description

Key Responsibilities:

• Coordinate and oversee the day-to-day operations of clinical trials.
• Recruit, screen, and enroll study participants.
• Obtain informed consent from study subjects.
• Maintain accurate and complete study documentation and records.
• Schedule and conduct study visits and follow-ups.
• Ensure compliance with study protocols, GCP, and regulatory guidelines.
• Collect, process, and ship biological samples as needed.
• Report adverse events and assist with IRB submissions.
• Communicate with sponsors, monitors, and regulatory agencies as required.
• Responsible for preparing and dispensing the investigational product (IP) according to randomization.
• Maintains blinding for other staff.

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