CRA / Sr CRA
Thermo Fisher Scientific · Remote
Clinical OperationsRemoteFull timeCompany career page
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Role summary
Thermo Fisher Scientific seeks a Clinical Research Associate to monitor and manage clinical trial sites, ensuring compliance with protocols, ICH-GCP guidelines, and regulatory standards. The role involves coordinating with investigative sites and cross-functional teams to maintain patient safety, data integrity, and study quality across pharmaceutical and biotechnology trials.
What they're looking for
- Bachelor's degree in Life Sciences, Nursing, or related healthcare field
- Relevant clinical research or monitoring experience in pharmaceutical, biotechnology, CRO, or healthcare setting
- Valid driver's license where applicable
- Knowledge of ICH-GCP guidelines and clinical trial regulatory requirements
- Proficiency with Microsoft Office and clinical trial management systems
- English language proficiency required
- Ability to travel 60-80% as required
What you'll be doing
- Conduct on-site and remote monitoring visits using risk-based monitoring approaches
- Review source documentation, case report forms, and study data for accuracy and compliance
- Perform site initiation, routine monitoring, and close-out visit activities
- Identify site process issues, perform root cause analysis, and support corrective actions
- Prepare monitoring reports and maintain study documentation in clinical trial management systems
Privacy & handoff
This role links to Thermo Fisher Scientific's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.