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Precision Medicine Group
Clinical Research Associate II/ Senior Clinical Research Associate
Remote · UK · Full time · Mid level
About the role
Monitor and own progress of clinical studies at investigative sites ensuring compliance with protocols and regulations. Coordinate activities for study setup and monitoring including regulatory submissions and site visits.
What you’ll do
• Monitor clinical studies at investigative sites. • Ensure studies follow protocol, SOPs, ICH-GCP. • Coordinate study setup activities. • Identify investigators and prepare regulatory submissions. • Conduct pre-study and initiation visits.
What you’ll bring
• 4-year degree or equivalent experience. • More than 1 year CRA experience in CRO or pharma. • Oncology experience essential. • Availability for up to 60% domestic travel. • Fluency in English.
Life at Precision Medicine Group
High CRA retention rates with a focus on quality of life and work/life balance. Smaller CRO with direct management support and employee influence.
About Precision Medicine Group
Precision Medicine Group combines clinical trial design, operational and medical expertise, biomarker and data analytics to advance precision medicine in oncology and rare diseases.