Clinical Research Associate II

🔥 1 minute ago

🌐 Belgium, Netherlands – Remote

infoinfo

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🗣️🇳🇱 Dutch Required

Where this job comes from

Posted on Precision Medicine Group's careers page, not through a job board

First seen by Remote Rocketship 1 minute ago

Logo of Precision Medicine Group

Precision Medicine Group

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

🎯 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 approach • Evidence of a client-focused approach • Availability for domestic travel, including overnight stays, up to approximately 50–60% • Fluency in English and Dutch • Candidates must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Lower than average number of protocols • Reasonable travel and improved work/life balance • Direct line management support • Opportunities to have influence and impact in a smaller CRO • Remote-based work arrangement • Equal Opportunity Employer

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