Clinical Research Associate I – Clinical Research Associate II

🔥 57 minutes ago

🇫🇷 France – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Precision For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• 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

• 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

• 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