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Precision for Medicine

Clinical Research Associate II - Remote

1w

Precision for Medicine

GB · Full-time · £45,000 – £65,000

About this role

Precision for Medicine is not your typical CRO. We cultivate our culture with extremely high CRA retention rates compared to industry averages. CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life.

You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully, your voice will be heard in a smaller CRO with influence and impact plus support from direct line management.

You will monitor and own the progress of clinical studies at investigative sites. Ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations. Coordinate all necessary activities required to set up and monitor a study.

Precision’s integrated offering combines novel clinical trial designs, operational and medical experts, biomarker and data analytics for precision medicine. We focus on rare diseases and oncology, revolutionizing cancer treatment with biomarkers and targeted trials. Employees feel appreciated with ideas valued and nurtured for positive change.

Requirements

  • 4-year college degree or equivalent experience
  • More than 1 year CRA experience within the CRO or pharmaceutical industry
  • Oncology experience, early phase experience desirable
  • Availability for domestic travel including overnight stays up to 50-60%
  • Fluency in English
  • Calm, thoughtful, and responsive when things don’t go as planned
  • Well-prepared for investigator meetings, site visits, or project team updates

Responsibilities

  • Monitor and own the progress of clinical studies at investigative sites
  • Ensure clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and applicable regulations
  • Coordinate activities to set up and monitor studies
  • Identify investigators
  • Help prepare regulatory submissions
  • Conduct pre-study and initiation visits
  • Identify potential study risks and propose mitigation solutions

Benefits

  • Extremely high CRA retention rates compared to industry averages
  • Lower than average number of protocols to become a protocol expert
  • Reasonable travel supporting work/life balance
  • Voice heard with influence and impact in smaller CRO
  • Support from direct line management
  • Fully home based working in the UK