Remote Study Coordinator - Part-Time Clinical Research

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

Descrizione del lavoro

A clinical research organization is seeking a detail-oriented Central Study Coordinator for a part-time position (24 hours per week) in Italy. This remote role involves supporting the planning, execution, and oversight of clinical research studies while ensuring compliance with regulatory standards. Ideal candidates should hold a Bachelor’s degree in a life sciences field, have experience in clinical research, and possess strong communication and organizational skills.

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 and trackers.
• Serve as a central point of communication.
• Assist with study start-up activities.
• Track enrollment and study timelines.
• Perform quality checks on study documents.
• Coordinate study meetings and prepare agendas.

Conoscenze

Detail-oriented

Excellent communication

Time-management

Organizational skills

Proficiency with study management systems

Microsoft Office Suite

Formazione

Bachelor’s degree in Life Sciences, Nursing, Public Health, or a related field

Descrizione del lavoro

A clinical research organization is seeking a detail-oriented Central Study Coordinator for a part-time position (24 hours per week) in Italy. This remote role involves supporting the planning, execution, and oversight of clinical research studies while ensuring compliance with regulatory standards. Ideal candidates should hold a Bachelor’s degree in a life sciences field, have experience in clinical research, and possess strong communication and organizational skills.