Clinical Research Associate

Role & Responsibilities
• Conduct off-site monitoring visits during study phases
• Perform Site Initiation Visits (SIVs) and ensure study readiness
• Review protocol prerequisites and site compliance
• Execute routine monitoring as per study monitoring plans
• Coordinate with sites for feasibility assessments
• Prepare and submit study-related reports (SIV, monitoring, close-out, etc.)
• Collect and manage essential trial documents
• Review trial documents for SOP, protocol, and regulatory compliance
• Train and mentor teams on ICH-GCP and regulatory updates
• Support internal and external audits and inspections

Qualifications & Experience
• Degree in Life Sciences, Pharmacy, or Clinical Research
• 1-3 years of experience as a Clinical Research Associate or equivalent
• Strong knowledge of ICH-GCP guidelines
• Experience in clinical trial monitoring and CRO operations
• Excellent documentation, communication, and coordination skills

Skills
• Proficient in ICH-GCP and regulatory compliance
• Strong organizational and time-management skills
• Ability to analyze clinical trial data and resolve issues
• Good problem-solving and decision-making skills
• Excellent communication skills (verbal and written)
• Detail-oriented with strong documentation skills

About the Company
• Veeda Clinical Research is a well-established CRO in India, supporting global and domestic clinical trials across multiple therapeutic areas, offering strong career-building opportunities for aspiring CRAs.