Clinical Research Associate FREELANCE

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

Descrizione del lavoro

A dedicated Contract Research Organization is seeking a Clinical Research Associate to join their team remotely in Catania, Italy. Responsibilities include conducting monitoring visits, writing reports, and ensuring data integrity. The ideal candidate has a relevant degree, experience in clinical monitoring, and a valid CRA certification. This role offers a dynamic work environment and opportunities for travel in Central-South Italy.

Servizi

Full remote job

Multicultural work environment

Competenze

• Proven experience in clinical monitoring.
• Proven GCP-ICH training.
• Actual CRA certification as per MoH decree 15/11/2011.

Mansioni

• Conduct and perform various monitoring visits according to SOPs.
• Write Monitoring Reports and manage site activities.
• Support the team on study submissions to ethics committees.

Conoscenze

Clinical monitoring

Organizational skills

Time management

Data integrity

Formazione

Bachelor’s degree/MD in technical-scientific field

Descrizione del lavoro

Social network you want to login/join with:

Clinical Research Associate FREELANCE, catania

col-narrow-left

Client:

Evidilya

Location:

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

8662617666420211712337122

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