Study coordinator clinical research

1 settimana fa


Torino, Italia ProPharma A tempo pieno

Position: Central Study Coordinator
Location: Remote, Italy
Employment Type: Part-time – 24 hours per week (Contract)
Clinical Research / Life Sciences
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.
Support day-to-day coordination of clinical study operations.
Assist with study start-up activities, including document collection and site readiness.
Perform quality checks on study documents to ensure compliance with GCP, SOPs, and regulatory standards.
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.
Bachelor’s degree in Life Sciences, Nursing, Public Health, or a related field.
~Proficiency with study management systems and Microsoft Office Suite.
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