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SpecialismClinical Research
Clinical operations teams run on people who have actually monitored sites, resolved findings and held a study to its timeline. We look for that evidence, not just a title.
Roles we recruit
- Clinical Research Associate (CRA I, II, Senior)
- Clinical Trial Manager
- Clinical Project Manager
- Study start-up specialist
- Clinical operations lead
- Trial master file (TMF) specialist
Skills and systems we screen for
- ICH-GCP
- Site monitoring and close-out
- Risk-based monitoring
- CTMS and eTMF systems
- Ethics committee and regulatory submissions
- Vendor and CRO oversight
What we ask in the screening call
- Therapeutic-area depth and phase exposure
- Number of sites and visits handled independently
- Audit and inspection experience
- Travel and relocation constraints
Regulatory frameworks
Reference points we use when briefing and screening.
- ICH-GCP
- EMA / CTR (EU)
- FDA (21 CFR)
- CDSCO (India)