Clinical Research Associate

Job Summary

Clinical Research Associate (CRA) Fresher

Key Responsibilities

• Assist in monitoring clinical trial sites under supervision
• Support maintenance of

  Trial Master File (TMF)

  and essential documents
• Assist in

  source data verification (SDV)

  and CRF review
• Coordinate with site staff for study-related activities
• Ensure compliance with

  ICH-GCP, SOPs, and study protocols

• Support reporting of deviations, adverse events, and issues

• Participate in site initiation, monitoring, and close-out activities (as trained)

• Maintain accurate and timely documentation

Eligibility / Qualifications

• Bachelor's or Master's degree in

  Life Sciences, Pharmacy, Nursing, or related field

• Fresher

  in clinical research
• Basic knowledge of

  clinical trial phases and GCP guidelines

• Willingness to learn and travel (if required)

Required Skills

• Good communication and coordination skills
• Strong attention to detail
• Basic computer skills (MS Word, Excel, Email)
• Time management and professionalism