Clinical Research Associate I / Clinical Research Associate II – Clinical Trial Services (Remote, Netherlands/Belgium)
Location: Remote – Netherlands / Belgium
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) specializing in oncology and rare disease clinical trials. We combine clinical trial execution, scientific expertise, laboratory capabilities, and advanced data analytics to accelerate the development of life-changing therapies. Our integrated approach ensures high efficiency, quality outcomes, and faster access to innovative treatments for patients.
We pride ourselves on our unique culture, high CRA retention, and collaborative environment. CRAs at Precision for Medicine enjoy manageable protocol loads, professional development opportunities, and a supportive work-life balance while making a meaningful impact on clinical trial success.
Role Overview
Precision for Medicine is seeking Clinical Research Associate I / Clinical Research Associate II (CRA I / CRA II) to join our remote Clinical Trial Services team in the Netherlands or Belgium. This role requires travel to clinical sites for morning monitoring visits and is ideal for candidates with oncology monitoring experience.
As a CRA, you will oversee the conduct, progress, and reporting of clinical studies, ensuring compliance with protocols, SOPs, ICH-GCP, and regulatory standards. This position provides exposure to protocol management, investigator interactions, regulatory submissions, and site monitoring activities, with opportunities for professional growth in oncology clinical trials.
Key Responsibilities
Monitor clinical trials at investigative sites to ensure compliance with protocols, regulations, and GCP standards.
Coordinate study start-up and site initiation activities, including regulatory submission support, pre-study visits, and investigator identification.
Identify study risks and propose mitigation strategies to ensure trial objectives are met.
Maintain accurate and high-quality documentation, including source data verification and query resolution.
Act as a primary point of contact for investigators, site staff, and cross-functional teams.
Contribute to continuous improvement of clinical trial processes and site performance.
Required Qualifications
Degree in Life Sciences or equivalent experience.
1+ year of CRA experience in a CRO, pharmaceutical, or biotech environment, or equivalent site management experience.
Proven experience managing oncology clinical trials.
Excellent organizational, communication, and interpersonal skills.
Fluency in English, Dutch, and French.
Availability for domestic travel, including overnight stays (approximately 50–60%); international travel may be required for senior-level roles.
Preferred Qualifications:
Experience in clinical trial start-up and site initiation activities.
Why Join Precision for Medicine?
Work in a CRO culture that values input, collaboration, and professional growth.
Manage oncology-focused clinical trials and gain expertise in protocol execution.
Maintain work-life balance with a manageable number of trial protocols.
Contribute meaningfully to the advancement of precision medicine and oncology therapies.
Application Notes
Applicants should be cautious of fraudulent recruitment activities. All official job offers will be communicated only through Precision for Medicine’s recruiting team following a formal interview process.
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Japan | Saitama |Tokyo :
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