Looking to build a career in clinical research, pharmacovigilance, or clinical operations? Precision For Medicine is hiring a Centralized Visit Report Reviewer I (CVRR I) in Bengaluru. This role is ideal for candidates with life sciences backgrounds and clinical trial exposure, offering hands-on involvement in monitoring visit report review, compliance, and risk assessment.

This opportunity is highly relevant for B.Pharm, M.Pharm, BSc, MSc, Nursing, and Medical graduates aiming to enter or grow in clinical trial management and CRO roles.

🧪 Key Responsibilities

• Review and approve clinical monitoring visit reports per SOPs and protocols
• Ensure consistency across studies and compliance with ICH-GCP guidelines
• Coordinate with clinical monitors for timely report submission and approvals
• Identify and escalate protocol deviations, safety concerns, and open action items
• Analyze clinical data, dashboards, and study trends for risk assessment
• Participate in project meetings and contribute to quality improvements
• Support audit readiness and regulatory compliance
• Assist in developing tools, reporting systems, and process enhancements

🎓 Eligibility Criteria

• Bachelor’s degree in Life Sciences / Pharmacy / Nursing / Medical fields
• Minimum 1 year experience in clinical monitoring or clinical trial management
• Strong knowledge of ICH-GCP and clinical development processes

🧠 Required Skills

• Excellent clinical report review and analytical skills
• Strong communication and stakeholder coordination
• Ability to extract insights from clinical systems and protocols
• Good time management and organizational abilities
• Capability to work independently and in cross-functional teams

💰 Salary & Benefits

• Estimated Salary: ₹5,00,000 – ₹8,00,000 per annum
• Exposure to global clinical trials and CRO operations
• Opportunity to work with cross-functional clinical teams
• Strong career progression in clinical research and regulatory domains

🚀 How to Apply

Application Link