Freelancer-Study Coordinator

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

Descrizione del lavoro

A leading clinical research organization is seeking a detail-oriented and proactive Central Study Coordinator for a part-time role in Italy. The position involves coordinating day-to-day clinical study operations, maintaining documentation, and ensuring compliance with regulatory standards. Applicants should have a Bachelor’s degree in Life Sciences or a related field and possess excellent communication and organizational skills. This remote opportunity is ideal for those looking to contribute to dynamic clinical research projects.

Competenze

• 1 year of experience as a CRA, CTA, or study coordination experience preferred.
• Strong understanding of clinical research processes.
• Ability to work in a team-oriented environment.

Mansioni

• Coordinate clinical study operations and communication between sites and teams.
• Maintain documentation and manage study activities.
• Perform quality checks on study documents and compliance.

Conoscenze

Good Clinical Practice (GCP)

Communication skills

Time-management

Organizational skills

Familiarity with study management systems

Proficiency in Microsoft Office Suite

Formazione

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

Descrizione del lavoro

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 remote opportunity within Italy 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.