Clinical Research Associate - freelance

JR Italy; Pistoia; In loco; EUR 30.000 - 50.000; Tempo pieno

Descrizione del lavoro

A leading Contract Research Organization is seeking a Clinical Research Associate for its team in Pistoia. The role involves conducting various site visits and ensuring data integrity while offering a full remote work option. Candidates should have a relevant degree and experience in clinical monitoring along with proven GCP-ICH training. Availability for travel in Central-South Italy is required.

Servizi

Full remote job

Multicultural, young and dynamic work environment

Competenze

• Proven experience in clinical monitoring required.
• GCP-ICH training must be completed.
• Actual CRA certification as per MoH decree 15/11/2011.

Mansioni

• Conduct SQV/Pre-study Visits and monitoring visits.
• Write Monitoring Reports and manage sites.
• Check data integrity throughout the study.

Conoscenze

Clinical monitoring experience

Excellent organizational skills

Time management skills

Formazione

Bachelor’s degree/MD in technical-scientific field

Descrizione del lavoro

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Clinical Research Associate FREELANCE, pistoia

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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:

8662617666420211712337160

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