Monitor clinical studies at investigative sites per protocol, SOPs, ICH-GCP.
Coordinate site setup and monitoring tasks (investigators, submissions, visits).
Manage 2-3 protocols on average; support PMs on larger trials.
Interact with clients, initiate payments, assist in proposals.
Domestic travel up to 50-60%; some roles may require international travel.

🎯 Requirements

4-year college degree or equivalent experience
2+ years CRA experience within a CRO
Experience monitoring Cardiology or Lupus studies
Domestic travel with overnight stays; up to 50-60% travel
Fluency in English and local language of country where position is based

🎁 Benefits

Discretionary annual bonus
Health insurance
401(k) with company match
Life insurance
Paid parental leave
Paid time off for sick leave and vacation

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