Clinical Research Associate FREELANCE

JR Italy; Venezia; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A leading Contract Research Organization is looking for a Clinical Research Associate to join their team in Venice. You will conduct site visits and monitor clinical trials, ensuring data integrity and compliance. This role offers a full remote work opportunity and a dynamic, multicultural work environment.

Servizi

Full remote work opportunity

Multicultural, young, and dynamic work environment

Competenze

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

Mansioni

• Conduct and perform SQV/Pre-study visits and monitoring visits.
• Write Monitoring Reports and perform site management.
• Check data integrity and support team submissions.

Conoscenze

Clinical monitoring experience

Excellent organizational skills

GCP-ICH training

Formazione

Bachelor's degree/MD in a relevant field

Descrizione del lavoro

Clinical Research Associate (Freelance) - Venezia

Client:

Evidilya

Location:

Venezia, Italy

Job Category:

Other

EU work permit required:

Yes

Job Reference:

8662617666420211712337111

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 the development and management of observational, pre-clinical, and clinical trials. We are looking for a:

Clinical Research Associate

To reinforce the Operational Italian Team.

Main Responsibilities:

1. Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, close-out visits, according to SOPs and study Monitoring Plan.
2. Write Monitoring Reports and perform site management, addressing follow-up activities.
3. Check data integrity.
4. Support the team in the submission of the study to ethics committees/IRBs.

Hard & Soft Skills:

1. Bachelor’s degree/MD or equivalent in a technical-scientific field.
2. Proven experience in clinical monitoring and relevant training in the field.
3. Proven GCP-ICH training.
4. Current CRA certification as per MoH decree 15/11/2011.
5. 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.