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

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.