Clinical Research Associate

Assist in monitoring clinical trial sites to ensure compliance with study protocols.

Support site initiation, routine monitoring, and close-out visits.

Verify clinical trial data against source documents (Source Data Verification – SDV).

Review Case Report Forms (CRFs/eCRFs) for accuracy and completeness.

Ensure proper maintenance of Investigator Site Files (ISF).

Check informed consent forms (ICFs) and ensure proper documentation.

Assist in identifying and reporting protocol deviations.

Support the documentation and reporting of Adverse Events (AEs) and Serious Adverse Events (SAEs).

Ensure compliance with ICH-GCP guidelines and applicable regulatory requirements.

Communicate with Principal Investigators (PIs), study coordinators, and clinical research teams.

Maintain trial-related documents and ensure data confidentiality.

Prepare monitoring visit reports under senior CRA supervision

Pay

₹240,000.00 - ₹430,000.00 per year

Benefits

Cell phone reimbursement

Paid sick time

Paid time off

Provident Fund

Work Location

In person