Clinical Research Coordinator

7 days ago

Nikol Ahmedabad Gujarat, India Medigence Solutions Pvt. Ltd. Full time

Job Responsibility:
❖ Lead and manage the day-to-day conduct of clinical trials at the site.

❖ Ensure adherence to study protocols, ICH-GCP guidelines, and regulatory requirements.

❖ Serve as the primary point of contact between the site and the sponsor/CRO.

❖ Prepare, submit, and maintain regulatory documents (e.g., EC/IRB submissions, clinical trial agreements).

❖ Ensure informed consent forms are accurate and up to date.

❖ Ensure Proper informed consent process is conducted.

❖ Resolve data queries and discrepancies.

❖ Maintain complete and accurate source documentation.

❖ Mentor and train junior coordinators or clinical staff.

❖ Delegate tasks effectively while maintaining overall oversight.

❖ Conduct internal study meetings and updates.

❖ Collaborate closely with investigators, sponsors, monitors, and site staff.

❖ Report trial progress, recruitment status, and site metrics regularly.

❖ Coordinate logistics for study visits, sample shipments, and drug/device accountability

Pay: ₹15,000.00 - ₹18,000.00 per month

**Benefits**:

- Paid sick time
- Paid time off

Application Question(s):

- Have you done B.pharm or M.pharm?

**Education**:

- Bachelor's (preferred)

**Location**:

- Nikol, Ahmedabad, Gujarat (required)

Work Location: In person

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