Clinical Research Associate - freelance

JR Italy; Como; In loco; EUR 30.000 - 50.000; Part-time

Descrizione del lavoro

A specialized Contract Research Organization is seeking a Clinical Research Associate to join their remote team in Italy. The role requires conducting site visits, ensuring data integrity, and supporting trial submissions. The ideal candidate should have proven clinical monitoring experience and a relevant degree. This position offers a multicultural and dynamic work environment.

Servizi

Full remote job

Multicultural work environment

Competenze

• Proven experience in clinical monitoring and training in the field.
• Proven GCP-ICH training.
• Current CRA certification as per MoH decree 15/11/2011.

Mansioni

• Conduct and perform SQV/Pre-study Visits and site initiation visits.
• Write Monitoring Reports and manage site activities.
• Check data integrity and support submission to ethics committees.

Conoscenze

Clinical monitoring

Organizational skills

Time management

Formazione

Bachelor’s degree/MD or equivalent

Descrizione del lavoro

Social network you want to login/join with:

Clinical Research Associate FREELANCE, como

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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:

8662617666420211712337126

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