Freelance Clinical Research Associate
We are looking for a Part-Time Freelance CRA to strengthen our clinical operations in Italy. Job Requirements:Bachelor's degree required – preferred qualification in life sciences or medical sciencesMinimum 3 years of experience of onsite monitoring activitiesPrevious experience in Cardiovascular Disease researchProfound knowledge of clinical research processes and medical terminologyExpert knowledge of ICH GCP, and international and local regulatory requirementsPassion for clinical researchEnglish language proficiency of minimum level C1 (ref.
CEFR) – fluent in written and spoken EnglishDriving license B and ability to travelJob Responsibilities:You would be primarily responsible for monitoring clinical trialsEnsuring that clinical trial is conducted, recorded, and reported in accordance with all applicable international and local regulations and guidelines, good practices, SOPs and Clinical Trial ProtocolEnsuring data quality and integrity meet acceptable clinical standardsGuaranteeing the rights and safety of patients involved in a study are protectedPerforming and coordinating all aspects of the clinical monitoring and site management processConducting remote and on-site visits to assess protocol and regulatory compliance and managing required documentationDeveloping collaborative relationships with investigational sites, acting as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability; and ensuring audit readiness. Serving as facilitator of Clinical Trial conduct in respective area in terms of identifying qualified sites and investigators, facilitating communication between sponsor and regulatory authorities and trial sites. What We Offer:Competitive Pay – Fair compensation based on skills and experience. Friendly environment – in a privately owned international company. Mentorship and Guidance – Support from senior team members to enhance learning. You can apply via the link or send a CV directly to: *******SanaClis is an equal opportunity and inclusive employerSeniority levelMid-Senior levelEmployment typePart-timeIndustriesResearch Services #J-18808-Ljbffr
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