Job Description

:

We are looking for passionate and detail-oriented

Clinical Research Associates (CRAs)

to join our growing team. Freshers who are eager to start their career in the clinical research field are encouraged to apply. The selected candidates will be responsible for assisting in the planning, monitoring, and execution of clinical trials as per regulatory and ethical standards.

Roles and Responsibilities:

Assist in planning, setting up, and monitoring clinical trials. Ensure clinical studies are conducted according to protocol, SOPs, ICH-GCP guidelines, and regulatory requirements. Collect, review, and verify clinical trial data for accuracy and completeness. Coordinate with investigators, ethics committees, and sponsors for trial documentation and approvals. Maintain trial master files and ensure all documents are updated and compliant. Conduct site visits (as required) to monitor trial progress and ensure protocol adherence. Prepare and maintain study reports, case report forms, and essential documents. Support data management and safety reporting activities. Collaborate with cross-functional teams including data managers, medical writers, and project coordinators.

Key Skills Required:

Strong understanding of clinical research concepts and GCP guidelines. Good communication and documentation skills. Attention to detail and ability to handle multiple tasks. Proficiency in MS Office and familiarity with clinical trial software . Willingness to learn and grow in the clinical research field.
Job Types: Full-time, Permanent, Fresher

Pay: ₹15,000.00 - ₹22,000.00 per month

Benefits:

Cell phone reimbursement Commuter assistance Flexible schedule Internet reimbursement Paid sick time Provident Fund
Work Location: In person