FSP CRA (Level I)
Thermo Fisher Scientific · Shanghai, China
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Role summary
Thermo Fisher Scientific seeks a Clinical Research Associate I to monitor investigational sites and manage clinical trial operations in Shanghai. The role involves conducting remote and on-site visits to ensure protocol compliance, manage documentation, and support clinical research across multiple sponsor environments.
What they're looking for
- Bachelor's degree in life sciences or registered nursing certification
- Minimal clinical monitoring experience (~2 years) in clinical trials or healthcare
- Valid driver's license where applicable
- Knowledge of ICH GCP guidelines and applicable regulations
- Strong written and oral communication skills
- Critical thinking and root cause analysis capabilities
- Organizational and time management skills
What you'll be doing
- Conduct risk-based site monitoring visits to assess protocol and regulatory compliance
- Review source documents, case report forms, and investigational product records for accuracy
- Document observations and escalate deficiencies to clinical management
- Initiate and close out clinical trial sites according to procedures
- Facilitate communication between investigative sites, sponsors, and internal teams
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.