Jobid: 3201556891 (0.11)
Overview
As a Clinical Research Associate II, you will remotely monitor oncology studies for Precision for Medicine with periodic site visits across Belgium or the Netherlands. You contribute to high-quality trial execution, ensuring compliance with protocol, SOPs and ICH-GCP while collaborating with cross-functional teams. You’ll work in a smaller CRO environment that values voice, impact, and work-life balance, with reasonable travel and direct management support. This role offers the chance to become a protocol expert and shape trial outcomes in oncology and rare diseases.
Arbeidsvoorwaarden / Benefits
- remote-based position
- reasonable travel
- supportive management
- focus on work-life balance
- high CRA retention culture
Verantwoordelijkheden
- Monitor and own progress of clinical studies at investigative sites
- Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP and regulations
- Coordinate start-up and monitoring activities (e.g., identify investigators, regulatory submissions, pre-study and initiation visits)
Belangrijkste vereisten
- Life science degree and/or equivalent experience
- 2+ years as CRA in a CRO or pharma/biotech setting or equivalent
- Experience managing oncology studies
- Site management or similar clinical research experience
- Excellent communication and organizational skills; team player; client-focused
- Fluency in English and Dutch; French a plus
- Availability for domestic travel up to 50-60% (international travel may be required)
- calm, thoughtful, and responsive under pressure
- proactive problem solving
- attention to detail
- ICH-GCP compliance
- SOPs and regulatory submissions
- study start-up activities
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