Monitor clinical studies at investigative sites; ensure protocol/SOP/ICH-GCP compliance.
Coordinate study setup and monitoring (investigators, regulatory submissions, pre-study/initiation visits).
Work with 2-3 protocols on average; support PMs; client interactions and payments.
Domestic travel up to 50-60%; some senior roles may require international travel.

🎯 Requirements

4-year college degree or equivalent experience.
2+ years CRA experience; CRA II; 4+ years for Sr CRA.
Experience monitoring oncology studies.
Domestic travel availability up to 50-60%.
English fluency; local language for non-English countries.

🎁 Benefits

Discretionary annual bonus.
Health, retirement, life, and disability insurance.
Non-vested 401(k) with company match.
Parental leave and paid time off.
Pay range: $91,500 – $166,100 USD.

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