Clinical Research Associate I/II

Precision Medicine Group

. 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, SOPs, and ICH-GCP standards, while effectively communicating with stakeholders and mitigating study risks. Proven ability to coordinate site activities and maintain high-quality outcomes in clinical research.

Highest-signal resume keywords

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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study MonitoringProtocol ComplianceSOP AdherenceRisk Identification and MitigationPre-Study and Initiation VisitsInvestigator Meeting PreparationStudy-Related Conflict ResolutionQuality Assurance in Clinical TrialsTravel Coordination for Site VisitsLife Science Degree

Soft Skills

Excellent Communication SkillsOrganizational SkillsTeam-Player CapabilityClient-Focused Approach

Industry Keywords

ICH-GCPCROPharmaceutical IndustryBiotech IndustryClinical Research

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, and 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 study-related difficulties and conflicts
Take responsibility for the quality and outcomes of work

Requirements

What you’ll need

Based in Paris or the Paris area, France
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 capability
Evidence of a client-focused approach
Fluency in English and, for non-English-speaking countries, the local language of the country where the position is based
Candidates must be legally authorized to work in the country of employment 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
Growth support
Remote-based work arrangement
Equal Opportunity Employer
Reasonable accommodation support for applicants with disabilities