Freelance Clinical Research Associate

1 settimana fa

Roma, Lazio, Italia JR Italy A tempo pieno
Social network you want to login/join with: Freelance Clinical Research Associate, Rome

Client:

SanaClis Location:

Rome, Italy Job Category:

Other EU work permit required:

Yes Job Reference:

527449314114194636833710 Job Views:

4 Posted:

11.03.2025 Expiry Date:

25.04.2025 Job Description:

We Are Hiring We are looking for a

Part-Time Freelance CRA

to strengthen our clinical operations in

Italy.

Preference will be given to candidates based in or around

Rome, Pisa, Livorno, Grosseto,

or

Florence. 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 the 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. *SanaClis is an equal opportunity and inclusive employer.

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