Clinical Research Associate FREELANCE

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

Descrizione del lavoro

A Contract Research Organization is seeking a Clinical Research Associate in Genova, Italy to conduct site visits and support clinical trials. The role requires a Bachelor’s degree, clinical monitoring experience, and current CRA certification. This is a full remote position offering a dynamic and multicultural working environment with travel in Central-South Italy.

Servizi

Full remote job

Multicultural work environment

Competenze

• Proven experience in clinical monitoring and trainings in the field.
• Current CRA certification as per MoH decree 15/11/2011.
• Availability to travel, especially in Central-South Italy.

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.

Conoscenze

Clinical monitoring

GCP-ICH training

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, genova

Client:

Evidilya

Location:

Genova, Italy

Job Category:

Other

EU work permit required:

Yes

Job Reference:

866261766642021171233717

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 on the submission of the study to ethics committees/IRBs.

Hard & Soft Skills:

• Bachelor’s degree/MD or equivalent in technical-scientific field.
• Proven experience in clinical monitoring and trainings 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.