Support clinical research studies by assisting with study documentation, data entry, participant coordination, and ensuring compliance with study protocols and regulatory guidelines.
Key Responsibilities:
- Assist in conducting clinical research studies as per protocol.
- Maintain and organize study documents and records.
- Perform accurate data entry and verify research data.
- Coordinate participant visits and follow-up appointments.
- Support informed consent documentation.
- Ensure compliance with ethical and regulatory requirements.
- Communicate with investigators, sponsors, and study participants.
- Help prepare reports and maintain study files.
Pay: ₹350,000.00 - ₹420,000.00 per year
Benefits:
- Paid sick time
- Provident Fund
Work Location: In person
