Clinical Research Associate

• Assist in monitoring clinical trials at investigational sites under supervision
• Ensure compliance with ICH-GCP guidelines, regulatory requirements, and company SOPs
• Support site initiation, routine monitoring, and close-out visits
• Help in verifying source data and case report forms (CRFs)
• Maintain study documentation and track trial progress
• Assist in identifying and resolving site issues and deviations
• Coordinate with investigators, site staff, and internal study team
• Participate in training programs and development activities
• Prepare visit reports and documentation under supervision
• Bachelor's or Master's degree in Life Sciences, Pharmacy, Nursing, Biotechnology, or a related field

Job Types: Full-time, Permanent, Fresher

Pay: ₹23,858.48 - ₹38,990.58 per month

Benefits:

• Health insurance
• Paid sick time
• Provident Fund

Work Location: In person