Clinical Research Associate - freelance

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

Descrizione del lavoro

A reputable contract research organization is seeking a Clinical Research Associate to join their team in Savona, Italy. The role involves conducting site visits and managing clinical trials remotely. Candidates should have a relevant degree, experience in clinical monitoring, and necessary certifications. This position offers a multicultural and dynamic work environment with full remote flexibility.

Servizi

Full remote job

Dynamic work environment

Competenze

• Proven experience in clinical monitoring is mandatory.
• Proven GCP-ICH training is required.
• Actual CRA certification according to MoH decree 15/11/2011 is needed.

Mansioni

• Conduct SQV/Pre-study Visits and monitoring visits.
• Write Monitoring Reports and perform site management.
• Support submission to ethics committees/IRBs.

Conoscenze

Clinical monitoring

Organizational skills

Time management

Data integrity checking

Formazione

Bachelor's degree/MD or equivalent

Descrizione del lavoro

Social network you want to login/join with:

Clinical Research Associate FREELANCE, savona

col-narrow-left

Client:

Evidilya

Location:

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

8662617666420211712337170

Job Views:

3

Posted:

27.08.2025

Expiry Date:

11.10.2025

col-wide

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