CRA I - FSP
Thermo Fisher Scientific · Mahārāshtra, India
Clinical OperationsFull timeCompany career page
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Role summary
Clinical Research Associate responsible for monitoring investigational sites, ensuring protocol compliance, and managing clinical trial documentation. Conducts on-site and remote visits, performs source data verification, and maintains regulatory compliance across study sites in India.
What they're looking for
- Master's degree in life sciences or pharmacy
- 1-2 years of independent onsite clinical monitoring experience
- Hands-on experience conducting site visits for clinical trials in India
- Knowledge of ICH-GCP guidelines and applicable regulations
- Understanding of medical terminology and therapeutic concepts
- Strong oral and written communication skills
- Interpersonal skills and customer focus orientation
What you'll be doing
- Monitor investigator sites using risk-based approaches and root cause analysis
- Conduct source data review, verification, and case report form assessments
- Assess investigational product inventory and maintain compliance records
- Initiate clinical trial sites and perform trial close-out activities
- Facilitate communication between investigative sites, clients, and internal teams
Privacy & handoff
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