Clinical Research Associate I – Clinical Research Associate II

Precision For Medicine

. Monitor and own the progress of clinical studies at investigative sites .

Posted 10/15/2026full-timeRemote • FranceJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing clinical studies, ensuring compliance with protocols, regulations, and standards, while effectively communicating and coordinating with investigative sites. Proven ability to identify risks and implement mitigation strategies in a client-focused environment.

Highest-signal resume keywords

Clinical Research Associate (CRA) ExperienceOncology Study ManagementRegulatory Submission PreparationSite Management ExperienceFluency in English and Local Language

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study MonitoringProtocol ComplianceSOPs and ICH-GCP KnowledgeRisk Identification and MitigationStudy Start-Up Activities

Soft Skills

Excellent Communication SkillsOrganizational SkillsConflict ResolutionTeam PlayerClient-Focused Approach

Industry Keywords

Life Science DegreeCRO ExperiencePharmaceutical IndustryBiotech IndustryDomestic Travel Availability

About the role

Key responsibilities & impact

Monitor and own the progress of clinical studies at investigative sites
Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, applicable regulations, and standards
Coordinate activities required to set up and monitor studies
Identify investigators
Help prepare regulatory submissions
Conduct pre-study and initiation visits
Travel to sites for monitoring visits
Identify potential study risks and propose mitigation solutions
Prepare for investigator meetings, site visits, and project team updates
Handle conflicts using resolution strategies
Take responsibility for work quality and outcomes

Requirements

What you’ll need

Life science degree and/or equivalent experience
1 year or more as a CRA in a CRO or pharmaceutical/biotech industry, or equivalent relevant experience and/or demonstrated competencies
Site management or equivalent experience in clinical research
Experience managing oncology studies
Availability for domestic travel including overnight stays, up to approximately 50–60% travel commitment
Excellent communication and organizational skills
Team player
Evidence of a client-focused approach
Fluency in English and the local language of the country where the position is based
Study start-up activities experience preferred
Must be legally authorized to work in France without employer sponsorship
Please apply in English

Benefits

Comp & perks

Lower than average number of protocols
Reasonable travel and improved work/life balance
Direct line management support
Opportunities for influence and impact in a smaller CRO
Regular Full-time employment