Hybrid Clinical Trial Operations Specialist

Syneos Health, Inc.; 's-Hertogenbosch; Hybrid; EUR 42,000 - 56,000; Full time

Job summary

Syneos Health, Inc. in the Netherlands is seeking a Clinical Trial Coordinator to join our team in a hybrid role, working from the Haarlem office three days per week.

The role involves supporting site management, TMF maintenance, document control, and collaboration with Clinical Monitoring staff across studies. You will ensure compliance with corporate policies and guidelines while coordinating logistics, tracking regulatory documents, and preparing meeting materials.

Qualifications

• Master's or Bachelor's degree in a biomedical field.
• Strong communication and interpersonal skills.
• Willingness to embrace new technologies.
• Based in the Netherlands; Haarlem office three days per week.

Responsibilities

• Perform activities in compliance with Corporate and Clinical Operations Policies, SOPs and Work Instructions.
• Assist Clinical Monitoring with site management and sponsor liaison for assigned studies.
• Create and maintain Trial Master File (TMF) and project files, including audits.
• Prepare and maintain site manuals, reference tools and other documents.
• Maintain clinical tracking data in databases and manage documents.
• Coordinate site supplies packaging, shipping and tracking.
• Arrange team meetings and record accurate minutes and actions.
• Handle receipt and disposition of Case Report Forms and queries as needed.
• Complete required training to stay current in clinical research.

Skills

Communication

Interpersonal skills

Tech-savvy

Education

Master's or Bachelor's degree in biomedical field

Job description

Syneos Health, Inc. in the Netherlands is seeking a Clinical Trial Coordinator to join our team in a hybrid role, working from the Haarlem office three days per week.

The role involves supporting site management, TMF maintenance, document control, and collaboration with Clinical Monitoring staff across studies. You will ensure compliance with corporate policies and guidelines while coordinating logistics, tracking regulatory documents, and preparing meeting materials.