Clinical Research Associate (CRA) – Home-Based in Amsterdam | IQVIA FSP | Reduced Travel. Our platform advertises a premier opportunity for an experienced CRA to join IQVIA’s dedicated Functional Service Provider (FSP) team in the Netherlands. This home-based role offers a unique single-sponsor partnership, focusing on cutting-edge therapies in Oncology, Neurology, Immunology, and Diabetes. With a competitive salary, company car, and only ~30% travel due to innovative remote monitoring, this position provides an exceptional work/life balance. If you have 12+ months of independent monitoring experience and fluency in Dutch and English, apply before September 29, 2025, to become a molecule expert with a global leader.
Background & Job Description
Our website is a specialized career board connecting professionals with top-tier opportunities in the life sciences sector. This listing is for a Clinical Research Associate (CRA) position with IQVIA in Amsterdam, Netherlands. We are an independent service and are not part of IQVIA’s recruitment team; we provide this information to help qualified candidates discover this role.
IQVIA is the world’s leading human data science company, formed by the merger of IMS Health and Quintiles. They are focused on using data, technology, and advanced analytics to help healthcare clients find unparalleled insights and develop better solutions for patients, ultimately driving healthcare forward.
This role is part of IQVIA’s unique Clinical Functional Service Provider (FSP) business. Unlike traditional CRA roles, our team is dedicated to a single sponsor partner, allowing for deep immersion into specific protocols and therapeutic areas. This model fosters a collaborative environment with a common goal of quality delivery. The CRA becomes an indication and molecule expert, contributing directly to the sponsor’s pipeline. This home-based position is designed for efficiency and impact, utilizing a ‘Fit for Purpose Monitoring’ strategy that incorporates remote monitoring, significantly reducing the need for on-site visits to approximately 30% travel. This approach creates a more sustainable career with a fantastic work/life balance, all while working on the forefront of new medicine development.
Clinical Research Associate (CRA) – Home-Based in Amsterdam | IQVIA FSP | Reduced Travel
Tasks and Responsibilities
Based on the official job description, the key responsibilities for this role are:
Site Management and Monitoring:
- Perform all aspects of site management and monitoring activities for approximately 10 assigned sites across the Netherlands.
- Conduct monitoring visits (both on-site and remote) in compliance with the study protocol, sponsor SOPs, ICH-GCP guidelines, and regulatory requirements.
- Create, maintain, and complete accurate monitoring visit reports and follow-up letters in a timely manner.
- Develop and manage site-specific action plans to address findings and ensure compliance.
Site Relationship and Training:
- Build and maintain strong, professional relationships with investigative site staff.
- Provide comprehensive protocol and study-specific training to assigned sites to ensure a clear understanding of study requirements.
- Work collaboratively with sites to adapt, drive, and track subject recruitment plans to meet enrollment targets.
Team Collaboration and Mentorship:
- Collaborate effectively with the dedicated sponsor team and your IQVIA line manager.
- If appropriate, participate in co-monitoring activities and provide training and mentorship to junior members of the CRA team.
Data and Compliance Oversight:
- Verify the accuracy and completeness of data recorded in Case Report Forms (eCRFs) against source documents.
- Ensure the protection of patient rights and safety by verifying that informed consent procedures are followed and that site staff are performing activities within their delegated authority.
- Manage essential document collection and maintenance to ensure site and study compliance.
Qualifications
Education and Certification:
- A Bachelor’s degree in Life Sciences (e.g., Biology, Chemistry, Pharmacy) is required.
- Alternatively, a nursing background (e.g., Registered Nurse) with equivalent experience is also acceptable.
- Certification from a clinical research academy (e.g., ACRP, SOCRA) is highly desirable and viewed as a strong asset.
Experience:
- A minimum of 12 months of independent, on-site monitoring experience as a CRA is mandatory.
- Proven experience handling multiple protocols and working across a variety of therapeutic drug indications is required.
- Demonstrated in-depth knowledge and practical application of ICH-GCP guidelines and local regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is essential.
- Prior experience in Oncology, Neurology, Immunology, and/or Diabetes therapeutic areas is a significant advantage.
Additional Information
Compensation and Benefits:
- Competitive salary and a comprehensive benefits package.
- Company car or a car allowance is provided.
- Permanent employment contract with IQVIA.
- Genuine career development opportunities, including dedicated training and a clear path for progression.
- Dedicated IQVIA Line Manager for support and career guidance.
Role Details:
- Work Model: Home-based with flexible working hours.
- Travel: Approximately 30% or less nationwide travel within the Netherlands. The model utilizes remote monitoring to reduce on-site visits.
- Protocol Allocation: Usually allocated to 1-2 protocols, allowing for deep therapeutic expertise.
- Site Load: Responsible for the management of approximately 10 sites.
- On-Site Requirement: Typically between 6 and 9 days on-site per month.
Application Requirements:
- Languages: Full professional fluency in both Dutch and English is mandatory (written and verbal).
- License: Must hold a full, clean driving license valid in the Netherlands.
- Skills: Must possess strong communication, written, and presentation skills. Excellent time management and the ability to work flexibly are essential.
How to Apply:
This advertisement is provided by our independent job board. All applications must be submitted through the official IQVIA careers portal. We recommend reviewing the original job posting (Job ID referenced in source material) for the most accurate details before applying. The closing date for applications is September 29, 2025.
Disclaimer: Our platform acts as an advertising venue for this job posting. We have compiled this information from public sources and strive for accuracy. However, all details, including responsibilities, benefits, and requirements, are subject to change by IQVIA. We are not involved in IQVIA’s recruitment process and cannot provide application status updates.
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