Clinical Job Opportunity at ICON | Apply Now
Clinical job opportunities in the clinical research industry continue to grow as organizations expand their global clinical development programs. ICON Careers is currently hiring a Clinical Site Associate in the Netherlands, offering professionals in life sciences an excellent opportunity to build expertise in clinical trial operations and progress toward a Clinical Research Associate (CRA) role. This remote position provides valuable exposure to clinical monitoring, site management, and regulatory compliance within a leading global clinical research organization.
- Job Position: Clinical Site Associate (CSA)
- Location: Utrecht, Netherlands – Remote
- Job ID: JR152585
About the Company
Clinical job seekers looking for opportunities with globally recognized clinical research organizations may find this role highly appealing. ICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to advancing clinical development through innovation, excellence, and scientific expertise. The company supports pharmaceutical, biotechnology, and medical device organizations worldwide by delivering comprehensive clinical research services. ICON fosters an inclusive work environment that values diversity, professional growth, and employee well-being.
Clinical Job Description
Clinical job responsibilities focus on supporting clinical trial operations and ensuring clinical site compliance throughout study execution. ICON Careers is seeking a Clinical Site Associate (CSA) to join its dynamic clinical research team. The role involves supporting clinical trial activities by maintaining site documentation, ensuring audit readiness, coordinating site communications, and assisting with site management activities.
This remote role is designed to develop into a Clinical Research Associate (CRA) position with travel responsibilities upon promotion, which is expected within approximately one year. Successful candidates will work closely with experienced CRAs and clinical trial teams while building practical monitoring experience.
Qualifications
Clinical job applicants should possess the following qualifications:
Required Education
Bachelor’s degree in a relevant field such as Life Sciences or Healthcare.
Preferred Experience
Previous experience in clinical research or a related field is preferred.
Required Skills
- Strong organizational skills.
- Excellent communication abilities.
- Ability to work independently and collaboratively.
- Strong attention to detail.
- Effective task prioritization skills.
- Fluency in Dutch and English.
- ICH-GCP Certification.
- Must be living in the Netherlands.
Clinical Job – Key Responsibilities
Clinical job duties include supporting clinical trial sites and ensuring operational excellence.
Site Support & Oversight
- Manage site-level communications in both Dutch and English.
- Coordinate site training activities and systems access.
- Support site readiness activities before and after site visits.
- Follow up on action items and operational requirements.
Document Management
- Maintain the Trial Master File (TMF).
- Ensure documentation accuracy and compliance.
- Support audit and inspection readiness activities.
Why Join ICON Careers?
Clinical job seekers interested in long-term growth within clinical research can benefit from ICON’s supportive and inclusive work culture. ICON is committed to fostering innovation, diversity, inclusion, and professional development. The company provides employees with opportunities to work on impactful clinical studies while developing skills that support long-term career advancement in the life sciences industry.
