Clinical Research Associate - freelance

JR Italy; Pordenone; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading Contract Research Organization is seeking a Clinical Research Associate to join their Italian team. The role involves conducting monitoring visits, writing reports, and ensuring data integrity. Candidates should have a Bachelor’s degree or MD, clinical monitoring experience, and active CRA certification. This is a full remote position in a dynamic work environment.

Servizi

Multicultural work environment

Dynamic team

Competenze

• 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.
• Active CRA certification as per MoH decree 15/11/2011.
• Excellent organizational and time management skills.

Mansioni

• Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, close-out visits.
• Write Monitoring Reports and perform site management.
• Check data integrity.
• Support the team in the submission of the study to ethics committees/IRBs.

Descrizione del lavoro

Social network you want to login/join with:

Clinical Research Associate FREELANCE, Pordenone

Client:

Evidilya

Location:

Pordenone, Italy

Job Category:

Other

EU work permit required:

Yes

Job Reference:

8662617666420211712337135

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 expertise 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 the submission of 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.
• Active 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.