Clinical Research Associate FREELANCE

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

Descrizione del lavoro

A leading Contract Research Organization in Udine is seeking a Clinical Research Associate to reinforce their operational team. This full remote position focuses on conducting monitoring visits, ensuring data integrity, and supporting ethics committee submissions. Ideal candidates will have a relevant degree, experience in clinical monitoring, and current CRA certification, along with excellent organizational skills.

Servizi

Multicultural, young, and dynamic work environment

Full remote job

Competenze

• Proven experience in clinical monitoring and relevant 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 monitoring visits according to SOPs.
• Write Monitoring Reports and perform site management.
• Check data integrity.

Conoscenze

Clinical monitoring

Time management

Organizational skills

Formazione

Bachelor’s degree/MD in a technical-scientific field

Descrizione del lavoro

Social network you want to login/join with:

Clinical Research Associate FREELANCE, Udine

Client: Evidilya

Location: Udine, Italy

Job Category: Other

EU work permit required: Yes

Job Reference:

8662617666420211712337118

Job Views:

3

Posted:

27.08.2025

Expiry Date:

11.10.2025

Job Description:

Evidilya, the dedicated Contract Research Organization of Sprim Health Group, operates as a full-service international organization specializing in developing and managing observational, pre-clinical, and clinical trials. We are 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 perform site management, addressing follow-up activities.
• Check data integrity.
• Support the team in submitting the study to ethics committees/IRBs.

Hard & Soft Skills:

• Bachelor’s degree/MD or equivalent in a technical-scientific field.
• Proven experience in clinical monitoring and relevant training in the field.
• Proven GCP-ICH training.
• Current 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.