Clinical Research Associate I/II

🔥 1 hour ago

🇫🇷 France – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🚫👨‍🎓 No degree required

👻 Ghost score 21%

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Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 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, 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

• 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

• 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