Clinical Research Associate - freelance

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

Descrizione del lavoro

A Contract Research Organization is seeking a Clinical Research Associate to join their Italian team. The role involves conducting various study visits and ensuring data integrity while supporting ethics submissions. Candidates must have a relevant degree, CRA certification, and strong organizational skills. The position offers full remote work in a dynamic environment.

Servizi

Full remote work opportunity

Multicultural, young, and dynamic work environment

Competenze

• 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.

Mansioni

• Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, close-out visits.
• Write Monitoring Reports and manage site activities.
• Support the team in submitting the study to ethics committees/IRBs.

Conoscenze

Clinical monitoring

Report writing

Data integrity checking

Organizational skills

Time management

Formazione

Bachelor’s degree/MD or equivalent in technical-scientific field

Descrizione del lavoro

Social network you want to login/join with:

col-narrow-left

Client:

Evidilya

Location:

Job Category:

Other

-

EU work permit required:

Yes

col-narrow-right

Job Reference:

8662617666420211712337145

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. 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 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 within Central-South Italy.

What We Offer:

• Full remote work opportunity.
• Multicultural, young, and dynamic work environment.