Clinical Trial Assistant

2 days ago

Hyderabad, India ClinSync Clinical Research Pvt Ltd. Full time

1. Ensure timely deliverables as assigned for achieving project milestones (e.g., Regulatory submission, IEC submissions, Correspondences & follow-up with principaI/ sponsor)

2.Provide regular report updates of the progress of clinical studies to the appropriate personnel.

3.Planning and conducting of pre-study site evaluation.

4. Coordinate with different stakeholders to ensure ICFs, relevant study Logs, CRFs etc. are prepared as per the approved protocol & in a timely manner.

5. Coordinate, Update and maintain site wise project related trackers.

6.Conduct clinical site feasibility and are as well involved in study visibility.

7. Coordinate for receipt and file, site communications, monitoring visit reports, data flow information.
- 1) Qualification
- BPharm/ MPharm

3) Need to travel to project sites as an when required.

4) Should have knowledge and understanding on Clinical research, Phases II- IV.

**Job Types**: Full-time, Regular / Permanent

**Salary**: ₹170,000.00 - ₹200,000.00 per year

**Benefits**:

- Health insurance
- Leave encashment
- Provident Fund

Schedule:

- Day shift
- Morning shift

**Education**:

- Bachelor's (preferred)

**Experience**:

- total work: 1 year (preferred)
- total: 1 year (preferred)

**Language**:

- English,Hindi,Telegu (preferred)

**Speak with the employer**

+91-XXXXXXXXXX

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