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Precision for Medicine is a clinical research organization (CRO) specializing in oncology and rare disease trials. They integrate clinical trial execution with scientific expertise, laboratory capabilities, and advanced data sciences to accelerate the development of life-changing therapies.
You will serve as a Clinical Research Associate, monitoring and owning the progress of clinical studies at investigative sites. Your responsibilities include 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 for study setup and monitoring, including identifying investigators, preparing regulatory submissions, conducting pre-study and initiation visits, and managing ongoing site relationships.
The role is remote-based with required travel to sites for monitoring visits, typically 50-60% travel commitment including overnight stays. You will work with a smaller CRO structure that emphasizes lower protocol loads per associate, enabling you to become a protocol expert. The company is known for high CRA retention rates and strong work-life balance.
You should be calm, thoughtful, and detail-oriented with the ability to stay ahead of challenges. You identify study risks proactively and propose mitigation strategies. You excel at preparation, communication, and conflict resolution, and take ownership of work quality and outcomes.
Minimum qualifications: Life science degree or equivalent experience; 1+ years as a CRA in a CRO, pharmaceutical, or biotech company (or equivalent clinical research experience); demonstrated experience managing oncology studies; availability for domestic travel with overnight stays. Fluency in English, Dutch, and French is required. Preferred: study startup activities experience.
