Responsibilities
(a) Site management
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Study site selection, initiation (SIV) and clinical monitoring.
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Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.
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Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.
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Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.
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Track study recruitment to ensure recruitment target is achieved in all studies.
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Conduct monitoring visit according to SDV plan and SOP;

address issues with sites and complete monitoring visit report in a timely manner coordinating.
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Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.
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Assemble site specific EC submission dossier, and ensure submission to EC.
Training
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Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.
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Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.




Documentation
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Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down. Maintain and update these documents in investigator files, trial master files.
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Prepare/complete study records' archiving according to protocol and sponsor requirements.
(b) Drug Safety
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Ensure safety information is disseminated to all sites according SOP and applicable regulations.
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Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.
(c) Finance and Administration
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Finalize budget and obtain signed contract from site, prior to site initiation visit.
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Ensure Study Payment Schedule is executed and retain relevant documents/receipts.
(d) Study Tools and system
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Update and maintain Study tools/systems in a timely manner.
3. Qualifications
3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major.
3.2 At least 8 year of CRA experience;

3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;

3.4 Good skills onMicrosoft Word, Excel, PPT and Outlook, etc.

📌 Contractor Cra_spain (Madrid)
🏢 Tigermed
📍 Madrid