Freelancer-Study Coordinator

21 ore fa


WorkFromHome, Italia Propharma A tempo pieno

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. #J-18808-Ljbffr



  • WorkFromHome, Italia Propharma A tempo pieno

    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...


  • WorkFromHome, Italia Propharma A tempo pieno

    A clinical research organization in Italy is seeking a part-time Central Study Coordinator to support clinical research studies. The role involves coordinating study activities, maintaining documentation, and ensuring compliance with regulatory standards. Candidates should hold a relevant Bachelor's degree and possess strong communication and organizational...


  • WorkFromHome, Italia Propharma A tempo pieno

    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...


  • WorkFromHome, Italia Propharma A tempo pieno

    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...


  • WorkFromHome, Italia Propharma A tempo pieno

    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...


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