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Precision for Medicine is a clinical research organization (CRO) specializing in oncology and rare disease trials. The company differentiates itself by integrating clinical trial execution with scientific expertise, laboratory capabilities, and advanced data sciences. Known for high CRA retention rates and strong work-life balance, the organization maintains lower-than-average protocol loads per CRA and provides reasonable travel expectations.
In this Clinical Research Associate II role, you will monitor and own the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported in compliance with protocol, SOPs, ICH-GCP guidelines, and all applicable regulations. You will coordinate all necessary activities required to set up and monitor studies, including identifying investigators, preparing regulatory submissions, conducting pre-study and initiation visits, and managing ongoing site relationships.
The position is remote-based with required travel to sites for morning visits, with an expected travel commitment of approximately 50–60% domestically (including overnight stays). International travel may be required for some senior-level positions. You will work with a smaller CRO structure where your voice is heard and you have direct support from line management.
Key responsibilities include identifying potential study risks and proposing mitigation strategies, maintaining meticulous attention to detail, managing conflict through proven resolution strategies, and taking ownership of work quality and outcomes. You will be well-prepared for investigator meetings, site visits, and project team updates, staying ahead of potential issues.
The ideal candidate is calm, thoughtful, and responsive under pressure, with strong problem-solving abilities and a client-focused approach. You will be a team player with excellent communication and organizational skills.
**Requirements:**
Minimum Required:
- Life science degree and/or equivalent experience
- 2+ years as a CRA in a CRO, pharmaceutical, or biotech industry, or equivalent relevant experience and demonstrated competencies in site management or clinical research
- Experience managing oncology studies
Other Required:
- Excellent communication and organizational skills; team player mentality
- Evidence of client-focused approach
- Availability for domestic travel including overnight stays (50–60% travel commitment; international travel possible for senior roles)
- Fluency in English and Dutch
- French is a plus
Preferred:
- Study start-up activities experience
