Clinical Research Associate - freelance

JR Italy; Firenze; In loco; EUR 35.000 - 45.000; Tempo pieno

Descrizione del lavoro

A Contract Research Organization is seeking a Clinical Research Associate to join its operational team in Italy. The role involves conducting and performing visits, managing site locations, and ensuring data integrity. Candidates should have a degree in a technical-scientific field, experience in clinical monitoring, and be certified as a CRA. This position offers a fully remote work environment alongside travel opportunities in Central-South Italy.

Servizi

Multicultural, young and dynamic work environment

Full remote job

Competenze

• Proved experience in clinical monitoring and proven trainings in the field.
• Actual CRA certification as per MoH decree 15/11/2011.
• Excellent organizational and time management skills.

Mansioni

• Conduct SQV/Pre-study Visits and monitoring visits according to study Monitoring Plan.
• Write Monitoring Reports and perform site management.
• Check data integrity and support submissions to ethics committees/IRBs.

Formazione

Bachelor’s degree/MD or equivalent in technical-scientific field

Strumenti

Proven GCP-ICH training

Descrizione del lavoro

Social network you want to login/join with:

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Client:

Evidilya

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

866261766642021171233714

Job Views:

3

Posted:

27.08.2025

Expiry Date:

11.10.2025

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Job Description:

Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:

Clinical Research Associate

To reinforce the Operational Italian Team

Main Responsibilities:

• Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, close out visits, according to SOPs and study Monitoring Plan
• Write Monitoring Reports and performing site management, addressing FU activities
• Check data integrity
• Support the team on the submission of the study to ethics committees/IRBs

Hard & Soft Skills:

• Bachelor’s degree/MD or equivalent in technical-scientific field
• Proved experience in clinical monitoring and proven trainings in the field
• Proven GCP-ICH training
• Actual CRA certification as per MoH decree 15/11/2011
• Excellent organizational and time management skills.

Additional requirements:

• Availability to travel especially in Central-South Italy

What we offer:

• Full remote job
• Multicultural, young and dynamic work environment