Clinical Research Associate II

🔥 0 minutes ago

🌐 Netherlands, Belgium – Remote

🇳🇱 Netherlands – Remote 🇧🇪 Belgium – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 20%

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 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, 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 morning visits • Identify potential study risks and propose mitigation solutions • Handle conflict using resolution strategies • Support investigator meetings, site visits, and project team updates

🎯 Requirements

• Life science degree and/or equivalent experience • 2 years 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 • Excellent communication and organizational skills • Team-player ability • Client-focused approach • Availability for domestic travel, including overnight stays, up to approximately 50–60% • Fluency in English and Dutch • French is a plus • Study start-up activities experience preferred • Candidates must be legally authorized to work in the country of employment without employer sponsorship • Please apply in English

🏖️ Benefits

• Extremely high CRA retention rates • Lower than average number of protocols • Reasonable travel • Work/life balance • Support from direct line management • Opportunity to have influence and impact • Remote-based work arrangement