Clinical Research Associate II

Precision For Medicine

Clinical 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.

Posted 7/2/2026full-timeRemote • 🇬🇧 United KingdomJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in monitoring and managing clinical studies, ensuring compliance with protocols, SOPs, and ICH-GCP standards. Possesses strong coordination skills for study setup and investigator engagement within the pharmaceutical industry.

Highest-signal resume keywords

Clinical Study MonitoringICH-GCP ComplianceOncology ExperienceCRA ExperienceRegulatory Submissions

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ManagementProtocol AdherenceSOP ComplianceInvestigator IdentificationStudy Setup Coordination

Industry Keywords

CROPharmaceutical IndustryEarly Phase ExperienceDomestic TravelFluency in English

Tech Stack

Tools & technologies

Google 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