SlipstreamJobs tracks this role from the company's public career site. Apply directly on the employer's site.
Precision for Medicine is a clinical research organization (CRO) specializing in oncology and rare disease studies. The company differentiates itself by integrating clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences. They emphasize strong CRA retention rates, lower-than-average protocol loads per associate, reasonable travel expectations, and a collaborative culture where individual voices are heard.
As a Clinical Research Associate II, you will monitor and own the progress of clinical studies at investigative sites, ensuring studies are conducted, recorded, and reported in accordance with protocol, SOPs, ICH-GCP guidelines, and all applicable regulations and standards. 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.
You will be based in Belgium or the Netherlands in a remote-based position with required travel to sites for morning visits. The role requires approximately 50-60% domestic travel commitment, including overnight stays. You will work closely with investigator teams, project teams, and internal stakeholders to identify and mitigate study risks, maintain protocol compliance, and ensure high-quality study outcomes.
The ideal candidate is calm, thoughtful, and responsive under pressure. You are well-prepared for investigator meetings, site visits, and project updates, staying ahead of potential issues. You have an impeccable eye for detail, strong problem-solving skills, and the ability to handle conflict constructively. You take ownership of work quality and outcomes.
**Requirements:**
Minimum Required:
- Life science degree and/or equivalent experience
- 2+ years as a CRA in a CRO or pharmaceutical/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 may be required for senior positions)
- Fluency in English and Dutch
- French is a plus
Preferred:
- Study start-up activities experience
