Remote Study Coordinator - Part-Time (Italy)

Propharma; Remoto; EUR 50.000 - 70.000; Part-time

Descrizione del lavoro

A clinical research company is seeking a detail-oriented Central Study Coordinator for a part-time position in Italy. The role involves supporting the planning and coordination of clinical studies, maintaining documentation, and ensuring compliance with regulatory standards. Candidates should have a Bachelor’s in Life Sciences and GCP knowledge, with preferred experience as a CRA or CTA. This remote opportunity is perfect for those looking to work in a dynamic environment.

Competenze

• 1 year of experience as a CRA, CTA, or study coordination experience preferred.
• Strong understanding of Good Clinical Practice (GCP) and clinical research processes.
• Ability to work effectively in an on-site, team-oriented environment.

Mansioni

• 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.

Conoscenze

Excellent communication

Time-management

Organizational skills

Proficiency with study management systems

Knowledge of Good Clinical Practice (GCP)

Formazione

Bachelor’s degree in Life Sciences

Strumenti

Microsoft Office Suite

Study management systems

Descrizione del lavoro

A clinical research company is seeking a detail-oriented Central Study Coordinator for a part-time position in Italy. The role involves supporting the planning and coordination of clinical studies, maintaining documentation, and ensuring compliance with regulatory standards. Candidates should have a Bachelor’s in Life Sciences and GCP knowledge, with preferred experience as a CRA or CTA. This remote opportunity is perfect for those looking to work in a dynamic environment.