Clinical Research Associate

• Assist in the initiation, monitoring, and closeout of clinical trial sites.
• Help prepare and review study materials, including patient recruitment documents, informed consent forms, and study protocol.
• Coordinate with site personnel to ensure that they have the necessary resources and training to conduct the study.
• Support efforts to recruit and retain patients for clinical trials by ensuring the study is conducted ethically and per protocol.
• Monitor patient enrollment and follow-up visits, ensuring compliance with the study timeline.
• Assist in the collection of clinical trial data and ensure proper documentation in the Case Report Form (CRF).
• Ensure the accuracy, completeness, and timeliness of data entry, and report discrepancies or inconsistencies.
• Participate in site monitoring visits (with a senior CRA or independently as experience grows).
• Ensure that sites are adhering to the study protocol, regulatory requirements, and GCP guidelines.
• Help resolve any issues found during monitoring visits, including site non-compliance, missing data, or patient safety concerns.

Job Types: Full-time, Permanent, Fresher

Pay: ₹22,885.55 - ₹43,331.46 per month

Benefits:

• Health insurance
• Paid sick time
• Provident Fund

Work Location: In person