Monitor progress of clinical studies at investigative sites.
Ensure studies are conducted, recorded and reported per protocol and ICH-GCP.
Coordinate site start-up activities: investigators, regulatory submissions, and initiation visits.
Conduct pre-study visits and initiation visits; support project teams.
Identify study risks and propose mitigations.
Travel up to 50-60% as required.

🎯 Requirements

4-year college degree or equivalent experience.
1+ year CRA experience in CRO/pharma.
Oncology experience desirable.
Willingness to travel up to 50-60% domestically.
Fluency in English.

🎁 Benefits

Fully home-based role in the UK.
Excellent work-life balance and supportive team.
Opportunity to become a protocol expert in a smaller CRO.
Impactful work in oncology and rare diseases.

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