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 sciences Minimum 3 years of experience of onsite monitoring activities Previous experience in Cardiovascular Disease research Profound knowledge of clinical research processes and medical terminology Expert knowledge of ICH GCP, and international and local regulatory requirements Passion for clinical research English language proficiency of minimum level C1 (ref.
CEFR) – fluent in written and spoken English Driving license B and ability to travel Job Responsibilities: You would be primarily responsible for monitoring clinical trials Ensuring 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 Protocol Ensuring data quality and integrity meet acceptable clinical standards Guaranteeing the rights and safety of patients involved in a study are protected Performing and coordinating all aspects of the clinical monitoring and site management process Conducting remote and on-site visits to assess protocol and regulatory compliance and managing required documentation Developing 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 employer Seniority level Mid-Senior level
Employment type Part-time
Industries Research Services
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