CRA (Level I)
Thermo Fisher Scientific · Remote
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Role summary
Thermo Fisher Scientific seeks a Clinical Research Associate I to monitor investigational sites, ensure protocol compliance, and manage clinical trial documentation. This remote-based position involves risk-based monitoring, data verification, and coordination with sponsor companies and research sites across multiple trials.
What they're looking for
- Bachelor's degree in life sciences or registered nursing certification
- Approximately 2 years clinical monitoring experience or equivalent
- Knowledge of ICH-GCP guidelines and applicable regulatory requirements
- Strong written and oral communication skills with medical personnel
- Proficiency with Microsoft Office and clinical trial management systems
- Critical thinking and root cause analysis capabilities
- Valid driver's license where applicable
What you'll be doing
- Conduct on-site and remote monitoring visits to assess protocol compliance and regulatory adherence
- Review case report forms, source documents, and investigational product records for accuracy and completeness
- Document monitoring observations and escalate deficiencies to clinical management with timely follow-up
- Initiate trial sites, conduct investigator meetings, and facilitate trial closeout activities
- Provide trial status updates and maintain communication between sites, sponsors, and internal teams
Privacy & handoff
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