Clinical Research Associate (CRA I / CRA II / Sr. CRA)
About the Role
Roles & Responsibilities
• Monitor investigator sites using risk-based monitoring (RBM)
• Ensure compliance with protocol, ICH-GCP, SOPs, and regulations
• Conduct site initiation, monitoring, and close-out visits
• Perform SDV, SDR, and CRF reviews for data accuracy
• Maintain essential documents and audit readiness
• Communicate with sites, sponsors, and project teams
• Prepare monitoring reports, follow-up letters, and status updates
Qualification
• Bachelor’s degree in Life Sciences or Registered Nursing
Experience
• 2+ years of experience as a Clinical Research Monitor
Skills
• Strong knowledge of ICH-GCP and clinical trial regulations
• Proficiency in MS Office and CTMS tools
About The Company
Thermo Fisher Scientific is a global leader in serving science, providing innovative solutions for life sciences, diagnostics, and applied materials. With a strong commitment to supporting researchers and healthcare professionals, Thermo Fisher offers a comprehensive range of tools and services that enable the advancement of scientific discovery.
AI Career Power Suite
Resume Analyst
Unlock refined AI insights.
Interested?
Frequently Asked Questions
Everything you need to know about the process