Clinical Research Associate

4 weeks ago


Pune, India Statistical Pharma Full time

Your responsibilities include, but are not limited to:

- Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial
- Is the frontline liaison between Statistical and sites to ensure successful collaboration, meeting Statistical

expectation on milestone and deliveries
- Manages assigned study sites and networks, if applicable, conducting phase I-IV protocols according to

the monitoring plan and Statistical procedures
- Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs
continuous training for amendments and new site personnel as required. Retrains site personnel as
appropriate
- Conducts continuous monitoring activities (onsite and remote). Implements site management activities to
ensure compliance with protocol, GCP, global and local regulations, global and local processes to
secure data integrity and patient safety
- Is accountable for continuously updating all electronic systems (global and local) relevant to perform job

functions
- Ensures that study milestones for sites responsible are met as planned (i.e., study start-up, recruitment,

database analyses, closeout, etc.)

**Salary**: ₹12,000.00 - ₹48,000.00 per month

**Benefits**:

- Cell phone reimbursement
- Internet reimbursement
- Work from home

Schedule:

- Day shift

Supplemental pay types:

- Performance bonus



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