CRA (Level I)
Thermo Fisher Scientific · Remote
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
Thermo Fisher Scientific seeks a Clinical Research Associate I to conduct remote and on-site monitoring of investigational sites across clinical trials. The role involves assessing protocol compliance, managing documentation, performing data verification, and coordinating between sites and sponsors to ensure regulatory adherence and subject safety.
What they're looking for
- Bachelor's degree in life sciences or registered nursing certification
- Approximately 2 years of clinical monitoring or clinical trial experience
- Strong knowledge of ICH-GCP guidelines and applicable regulations
- Proficiency with Microsoft Office and ability to learn clinical trial management systems
- Excellent written and oral communication skills with medical terminology competency
- Critical thinking and root cause analysis capabilities
- Valid driver's license where applicable
What you'll be doing
- Conduct risk-based site monitoring visits to assess protocol compliance and data accuracy
- Review source documents, case report forms, and investigational product records; document findings in reports
- Identify site process failures and develop corrective/preventive actions to achieve compliance
- Initiate trial sites and facilitate investigator meetings; perform trial closeout and material retrieval
- Maintain communication between investigative sites, sponsor companies, and internal teams; provide status updates
Privacy & handoff
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