Central Study Coordinator

Negotiable
  1. Interim/Contract
Amsterdam, Nederland
  1. Clinical Operations, Clinical Trial Administration
Posted: 12/09/2025
BBBH27917

Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation!

Hobson Prior is seeking a Central Study Coordinator to join a clinical research team. In this role, you will act as a key point of contact between research sites and study participants, ensuring smooth study delivery and an excellent patient experience. You will coordinate daily activities, manage study documentation, and maintain quality standards while supporting the overall success of clinical trials. This is a remote position with minimal travel requirements.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Guide patients through the study process, including explaining informed consent.
  • Schedule and coordinate assessments, appointments, and communications for patients and study teams.
  • Maintain accurate study records and enter data into relevant systems.
  • Address and resolve issues to improve the study experience for patients and investigators.
  • Perform quality checks on data and ensure timely entry into systems.
  • Respond to queries and support data collection best practices.
  • Monitor compliance with safety reporting and escalate issues when necessary.
  • Build strong relationships with patients, investigators, and study teams.
  • Manage payments for study-related activities as needed.
  • Stay inspection-ready by keeping all documentation and trackers up to date.

Key Skills and Requirements:

  • Strong organizational and time management skills.
  • Ability to navigate and troubleshoot clinical technologies.
  • Clear communication and problem-solving abilities.
  • Familiarity with clinical research processes and medical terminology.
  • Understanding of patient safety and ethical considerations in clinical trials.
  • Experience in data management and query resolution.
  • Certification as a Clinical Research Coordinator (CCRC) is preferred but not required.

For more information, please contact Antonia Ray.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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