Full Time

Senior Clinical Research Associate (Sr. CRA)

REV Clinical
Gujrat
Competitive Salary
Posted 20/01/2026

About the Role

Role & Responsibilities

  • Lead site monitoring activities across multiple clinical trials

  • Ensure compliance with ICH-GCP, SOPs, and regulatory requirements

  • Perform site initiation, monitoring, and close-out visits

  • Review CRFs, source documents, and resolve data queries

  • Mentor junior CRAs and CTAs

Qualification

  • Bachelor’s / Master’s in Life Sciences, Pharmacy, Nursing, or related field

    Experience

    • 4–6 years of clinical monitoring experience in a CRO or pharmaceutical company

    Skills

    • Strong knowledge of ICH-GCP and clinical trial regulations

    • Excellent documentation and communication skills

    • Leadership and problem-solving abilities

    About Company

    REV Clinical (formerly CBCC Global Research) is a rapidly growing CRO delivering high-quality clinical research services globally.

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Senior Clinical Research Associate (Sr. CRA) at REV Clinical | Jobslly