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Clinical Research Associate II
Precision For MedicineClinical Research Associate II at Precision for Medicine, monitoring clinical studies and ensuring regulatory compliance in the UK. Involves managing sites, coordinating studies, and promoting positive culture.
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Monitor and own the progress of clinical studies at investigative sites
- Ensure clinical studies are conducted and reported per protocol, SOPs, ICH-GCP
- Coordinate all activities required to set up and monitor a study (i.e., identify investigators, regulatory submissions, conduct visits)
Requirements
What you’ll need- 4-year college degree or equivalent experience
- More than 1 years CRA experience within the CRO or pharmaceutical industry
- Oncology experience, early phase experience desirable although not essential
- Availability for domestic travel including overnight stays (50-60% travel commitment)
- Fluency in English
Benefits
Comp & perks- Precision’s uniquely integrated offering enables the science of precision medicine
- Cultivating a positive work culture
- High CRA retention rates
- Low travel commitments with flexible life balance
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Clinical Study ManagementProtocol AdherenceSOP ComplianceInvestigator IdentificationStudy Setup Coordination