Clinical Research Associate

4 days ago

Sevasi Vadodara Gujarat, India Anjna Hospital & Clinisearch Pvt.Ltd Full time

Key Responsibilities

1. To obtaining Inform Consent Form.

2. To request and maintain accountability of all study related documents.

3. To check all study related documents for its legibility, accuracy and completeness.

4. To solve QA/RGA queries.

5. To conduct study initiation meeting.

6. To supervise all ongoing study procedures including screening, check-in, dosing, blood collection and sample separation.

10. To prepare and display study information details.

11. To supervise meal distribution.

12. To supervise water and posture restriction.

13. To participate in dosing procedure.

14. To Compile Trial Master File.

15. To operate and maintain breath alcohol analyzer.

17. To prepare study related labels.

18. Any other administrative or system related activities has assigned by the Head
- Clinical or PI.

19. To check the raw data before Quality Assurance check.

20. To monitor the Bio-Waste management.

21. To make Entry in CRF (Case record form).

22. To handle the IMP.

23. To participate in dosing procedure.

24. To prepare study related labels (for IMPs/Other).

25. Any other assigned work allotted by Group Leader/Head Clinical/PI.

26. Report any areas of concern they have relating to the quality system to their line manager, Directors, QAU-Head.

27. To prepare the work related SOPs (Standard Operating Procedures) and perform all activities as per SOP (Standard Operating Procedures).

Pay: ₹15,000.00 - ₹20,000.00 per month

**Benefits**:

- Provident Fund

Schedule:

- Day shift
- Morning shift
- Night shift

Supplemental Pay:

- Overtime pay
- Performance bonus

**Education**:

- Bachelor's (preferred)

**Experience**:

- total work: 1 year (preferred)

**Location**:

- Sevasi, Vadodara, Gujarat (preferred)

Work Location: In person

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