Clinical Research Jobs at Precision for Medicine
Precision for Medicine is hiring Clinical Research Associate I / Clinical Research Associate II (CRA I / CRA II) professionals in the Netherlands for remote-based roles with site travel. The Clinical Research Jobs are ideal for CRAs with oncology monitoring experience who are seeking strong work–life balance, lower protocol burden, and the chance to make a meaningful impact within a specialized, science-driven CRO focused on Oncology and Rare Diseases.
Job Details:
- Job Title: Clinical Research Associate I / Clinical Research Associate II
- Location: Netherlands (Remote-based with site visits)
- Employment Type: Full-time
- Work Mode: Remote + Domestic Site Travel
- Therapeutic Area: Oncology, Rare Disease
- Travel Requirement: ~50–60% domestic travel
- Language Requirement: English, Dutch & French
About the Company:
Precision for Medicine is a next-generation Contract Research Organization (CRO) that integrates clinical trial execution, deep scientific expertise, laboratory services, and advanced data sciences. With a strong focus on Oncology and Rare Diseases, the organization is known for exceptional CRA retention, manageable workloads, protocol ownership, and a collaborative culture where every voice matters.
Educational Requirements for the Clinical Research Associate Role:
- Bachelor’s degree in Life Sciences or related field
- Equivalent clinical research experience will be considered
Key Responsibilities of the Clinical Research Associate:
- Monitor and manage clinical trial activities at investigative sites
- Ensure trials are conducted in compliance with ICH-GCP, SOPs, protocols, and regulatory requirements
- Perform site qualification, initiation, monitoring, and close-out visits
- Support study start-up activities including regulatory submissions
- Identify study risks and proactively implement mitigation strategies
- Maintain high-quality documentation and reporting
- Act as a primary liaison between sites, sponsors, and internal teams
- Ensure patient safety, data integrity, and protocol adherence
Skills Required for the Clinical Research Associate Role:
- Minimum 1+ year experience as a CRA (CRO or pharma/biotech)
- Proven oncology study monitoring experience
- Strong organizational, communication, and problem-solving skills
- High attention to detail and quality ownership
- Ability to manage conflict and resolve site-level challenges
- Client-focused mindset and team-oriented approach
- Willingness to travel domestically with overnight stays
- Fluency in English, Dutch, and French
Benefits of the Clinical Research Jobs:
- Excellent work–life balance with reasonable travel expectations
- Lower protocol load enabling true protocol expertise
- High CRA retention and strong managerial support
- Opportunity to work on cutting-edge oncology and rare disease trials
- Voice and influence within a smaller, agile CRO
- Career growth and exposure to advanced clinical research technologies
- Supportive, people-first organizational culture
