Clinical Research Associate I / Clinical Research Associate II – Clinical Trial Services (Remote, Belgium/Netherlands)
Location: Remote – Belgium / Netherlands
Job Type: Full-time
Division: Precision for Medicine
Business Unit: Clinical Solutions
Requisition Number: 6309
About Precision for Medicine
Precision for Medicine is a leading contract research organization (CRO) dedicated to accelerating life-changing therapies in oncology and rare diseases. By integrating clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data analytics, we enhance the speed, success rate, and efficiency of drug development. Our collaborative culture, high CRA retention, and focus on work-life balance ensure employees thrive while making meaningful contributions.
Role Overview
Precision for Medicine is seeking Clinical Research Associate I / Clinical Research Associate II (CRA I / CRA II) to join our Clinical Trial Services team in Belgium or the Netherlands. This fully remote position requires travel to clinical sites for morning monitoring visits. The CRA will be responsible for overseeing clinical study progress, ensuring trials comply with protocols, SOPs, ICH-GCP guidelines, and all applicable regulations.
This role is ideal for candidates with oncology clinical trial experience, offering opportunities to become a protocol expert while working in a supportive, smaller CRO environment.
Key Responsibilities
Monitor and manage clinical trials at investigative sites, ensuring adherence to protocols, regulatory standards, and GCP guidelines.
Coordinate study start-up and site initiation activities, including investigator identification, regulatory submission preparation, and pre-study visits.
Identify potential study risks and propose mitigation strategies to ensure study objectives are met.
Maintain high-quality study documentation, including source data verification, query resolution, and accurate reporting.
Serve as a point of contact for sites, sponsors, and cross-functional teams to address issues efficiently.
Support oncology-focused clinical trials and contribute to continuous process improvement initiatives.
Ensure all site and trial activities align with organizational quality standards and regulatory compliance.
Required Qualifications
Degree in Life Sciences or equivalent experience.
Minimum 1+ year of CRA experience in a CRO, pharmaceutical, or biotech environment; relevant site management experience is also considered.
Proven experience in managing oncology clinical trials.
Excellent organizational, communication, and interpersonal skills.
Client-focused approach and ability to work collaboratively within cross-functional teams.
Availability for domestic travel, including overnight stays (approximately 50–60%); international travel may be required for senior-level positions.
Fluency in English, Dutch, and French.
Preferred Qualifications:
Experience in clinical trial start-up activities and site initiation.
Why Join Precision for Medicine?
Work in a CRO that prioritizes employee growth, input, and influence.
Gain exposure to precision oncology trials and become a subject matter expert in protocol execution.
Maintain a strong work-life balance with a reasonable number of trial protocols.
Be part of a culture that values collaboration, mentorship, and professional development.
Application Notes
Applicants should be aware of fraudulent recruitment activity. All formal job offers from Precision for Medicine will come directly from our official recruitment team following a structured interview process.
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