Study coordinator clinical research

1 settimana fa

Sant'Ambrogio di Torino, Italia ProPharma A tempo pieno

Position: Central Study CoordinatorLocation: Remote, ItalyEmployment Type: Part-time – 24 hours per week (Contract)Clinical Research / Life SciencesWe 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.~

  • 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...

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    Sant'Ambrogio di Torino, Italia ProPharma A tempo pieno

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