Desgraciadamente este trabajo no está activo.

Study Coordinator

Position: Central Study CoordinatorLocation: Seville, Spain (On-site)Employment Type: Part-time – 24 hours per week

Descripción del empleo

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.

Información extra

Status
Inactiva
Estudios requeridos
E.S.O
Localización
Seville
Tipo de contrato
Trabajo estudiantes
Carnet de conducir
No
Vehículo
No
Carta de motivación
No
Idiomas
Español

Trabajo estudiantes | E.S.O