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This position was posted on April 14, 2026 and is likely no longer accepting applications. We've kept it here for historical reference. Check out the similar jobs below!
Job Overview
Location
Remote, Belgium
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 14, 2026
Full Job Description
đź“‹ Description
- • As a Clinical Research Associate I/II at Precision Medicine Group, you will play a critical role in advancing life-changing therapies in oncology and rare diseases by ensuring clinical trials are conducted with the highest standards of quality, compliance, and scientific rigor.
- • Your day-to-day responsibilities include monitoring clinical study progress at investigative sites, ensuring adherence to protocol, SOPs, ICH-GCP, and regulatory requirements; coordinating site setup activities such as investigator identification and regulatory submissions; conducting pre-study and initiation visits; and maintaining accurate documentation throughout the trial lifecycle.
- • You will join a mission-driven, innovative CRO that integrates clinical trial execution with deep scientific expertise, laboratory capabilities, and advanced data sciences—setting it apart from traditional CROs through its focus on oncology and rare disease therapeutics.
- • In this role, you will develop deep protocol expertise due to a lower-than-average protocol load, gain significant influence and visibility within a supportive team environment, and grow your career through meaningful contributions to impactful studies, all while benefiting from strong work-life balance and high retention rates reflective of a positive, people-first culture.
🎯 Requirements
- • Life science degree and/or equivalent experience
- • 1 year or more of experience as a CRA in a CRO, pharmaceutical, or biotech setting, or equivalent relevant experience in clinical research or site management
- • Demonstrated experience managing oncology studies
- • Fluency in English, Dutch, and French
- • Availability for domestic travel including overnight stays, up to approximately 50-60% of the time
🏖️ Benefits
- • Lower-than-average number of protocols, allowing you to become a true protocol expert
- • Reasonable travel commitments supporting improved work-life balance
- • A culture where your voice is heard and you can have meaningful impact, supported by direct line management
- • Extremely high CRA retention rates compared to industry averages, reflecting a positive and enjoyable work environment
- • Opportunity to contribute to life-changing therapies in oncology and rare diseases through integration of clinical, scientific, and data-driven expertise
Skills & Technologies
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About Precision Medicine Group
Precision Medicine Group (PMG) is a leading life sciences consulting firm dedicated to accelerating the development and commercialization of precision medicine. They offer a comprehensive suite of services, including strategy, market access, regulatory affairs, and commercialization support. PMG partners with pharmaceutical, biotechnology, and diagnostic companies to navigate the complex landscape of personalized healthcare. Their expertise spans various therapeutic areas and advanced molecular technologies. By leveraging deep scientific knowledge and market insights, PMG helps clients optimize their drug development pipelines, secure regulatory approvals, and successfully launch innovative therapies. They are committed to advancing patient care through the power of precision medicine, ensuring that the right treatments reach the right patients at the right time.
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