Study Coordinator

Position: Central Study Coordinator

Location: Seville, Spain (On-site)

Employment Type: Part-time – 24 hours per week (Contract)

Industry: Clinical Research / Life Sciences

About the Role

We are seeking a detail-oriented and proactive Central Study Coordinator to support the planning, execution, and oversight of clinical research studies. This on-site role in Seville serves as a central operational hub—coordinating study activities, maintaining study documentation, assisting site teams, and ensuring all study processes align with regulatory and sponsor requirements.

This position is ideal for candidates looking for a part-time role within a dynamic clinical research environment.

Key Responsibilities

- Support day-to-day coordination of clinical study operations.
- Maintain study documentation, trackers, logs, and study management systems.
- Serve as a central point of communication between study sites, vendors, and internal teams.
- Assist with study start-up activities, including document collection and site readiness.
- Track enrollment, site performance metrics, and study timelines.
- Perform quality checks on study documents to ensure compliance with GCP, SOPs, and regulatory standards.
- Coordinate study meetings, prepare agendas, and document meeting minutes.
- Support monitoring activities by assisting with follow-ups, reconciliation tasks, and issue resolution.
- Contribute to the development and review of study materials such as training guides, manuals, and plans.

Qualifications

- Bachelor’s degree in Life Sciences, Nursing, Public Health, or a related field.
- 1 year of experience as a CRA, CTA, or study coordination experience preferred.
- Strong understanding of Good Clinical Practice (GCP) and clinical research processes.
- Excellent communication, time-management, and organizational skills.
- Proficiency with study management systems and Microsoft Office Suite.
- Ability to work effectively in an on-site, team-oriented environment.