Clinical Research Associate - freelance

JR Italy; Plasencia; In loco; EUR 35.000 - 55.000; Tempo pieno

Descrizione del lavoro

A multinational Contract Research Organization is seeking a Clinical Research Associate to strengthen their Operational Italian Team. The role involves conducting monitoring visits, ensuring data integrity, and supporting ethical submissions. Candidates should have a relevant degree, clinical monitoring experience, and excellent organization skills. This is a full remote position with a dynamic work environment.

Servizi

Full remote job

Multicultural, young, and dynamic work environment

Competenze

• Proven experience in clinical monitoring and relevant training in the field.
• Excellent organizational and time management skills.

Mansioni

• Conduct and perform SQV/Pre-study Visits and monitoring visits.
• Write Monitoring Reports and manage site activities.
• Check data integrity.

Conoscenze

Clinical monitoring experience

Time management

Organizational skills

Formazione

Bachelor’s degree in a technical-scientific field

Current CRA certification as per MoH decree 15/11/2011

Descrizione del lavoro

Client: Evidilya

Location:

Job Category:

Other

EU work permit required:

Yes

Job Reference:

8662617666420211712337132

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, and close-out visits according to SOPs and study Monitoring Plan.
• Write Monitoring Reports and manage site activities, including 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.