Job Description

Patient Care & Recruitment:

• Screen, enroll, and educate patients about trial protocols, manage appointments, and collect follow-up data.

Protocol Adherence:

• Ensure all study activities (drug administration, data collection) strictly follow the study protocol and Good Clinical Practice (GCP).

Data Management:

• Collect, enter, and manage accurate study data; communicate with labs about results.

Regulatory Compliance:

• Work with Institutional Review Boards (IRBs) and sponsors to maintain compliance with laws and regulations.

Team Collaboration:

• Work with doctors, nurses, and other staff; train new personnel; and communicate with sponsors and regulatory bodies.

Administrative Tasks:

• Manage study budgets, supplies, and development of recruitment materials.

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