Job Description

About the Role

We are looking for a meticulous and motivated Clinical Research Associate (Trainee) to join our clinical research team. This entry-level role offers hands-on experience in monitoring and coordinating clinical trials, ensuring they comply with regulatory standards and protocol guidelines. The trainee will work closely with senior CRAs and clinical site staff to support the successful execution of clinical studies.

Key Responsibilities

Assist in conducting site visits to monitor clinical trial progress, compliance, and data accuracy. Support documentation and management of clinical trial materials and regulatory submissions. Help ensure the protection and well-being of trial participants by adhering to Good Clinical Practice (GCP) guidelines. Collect, verify, and review case report forms (CRFs) and source data for completeness and accuracy. Coordinate with investigators, site staff, and sponsors to facilitate smooth trial operations. Participate in training and development sessions to build clinical trial management skills. Assist in preparing monitoring reports and trial documentation. Support the tracking of patient enrollment and follow-up activities. Maintain confidentiality and comply with ethical and regulatory requirements.
Qualifications

Bachelor's degree in Life Sciences, Pharmacy, Nursing, or related field. Interest in clinical research and healthcare. Strong attention to detail and organizational skills. Basic understanding of clinical trial processes and regulations is a plus. Good communication and interpersonal skills. Proficient in Microsoft Office applications. Ability to work independently and as part of a team. Willingness to travel as required for site visits.
Job Types: Full-time, Permanent, Fresher

Pay: ₹9,591.96 - ₹20,407.06 per month

Work Location: In person