Clinical Research Associate - freelance

JR Italy; Varese; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A Contract Research Organization is looking for a Clinical Research Associate to join its team in Italy. This full remote position requires a Bachelor's degree or MD in a technical field, along with proven experience in clinical monitoring and GCP-ICH training. The ideal candidate will have excellent organizational and time management skills, with availability to travel in Central-South Italy.

Servizi

Multicultural, young, and dynamic work environment

Full remote job

Competenze

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

Mansioni

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

Conoscenze

Clinical monitoring experience

Excellent organizational skills

Time management skills

Formazione

Bachelor’s degree or MD in technical-scientific field

Descrizione del lavoro

Social network you want to login/join with:

Clinical Research Associate FREELANCE, varese

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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:

8662617666420211712337121

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