Clinical Research Associate - freelance

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

Descrizione del lavoro

A Contract Research Organization in Lecco is seeking a Clinical Research Associate to join their operational team. The role involves conducting clinical monitoring visits and ensuring data integrity, with a need for a Bachelor's degree, CRA certification, and availability to travel. This position offers a remote work opportunity in a dynamic multicultural setting.

Servizi

Full remote work opportunity

Dynamic work environment

Competenze

• Proven experience in clinical monitoring.
• Current CRA certification as required.
• Availability to travel in Central-South Italy.

Mansioni

• Conduct SQV/Pre-study Visits and monitoring visits.
• Write Monitoring Reports and perform site management.
• Support the team in submitting studies to ethics committees.

Conoscenze

Clinical monitoring experience

Organizational skills

Time management

Formazione

Bachelor’s degree or equivalent in a technical-scientific field

MD or equivalent

Strumenti

GCP-ICH training

CRA certification

Descrizione del lavoro

Social network you want to login/join with:

Clinical Research Associate FREELANCE, Lecco

Client: Evidilya

Location: Lecco, Italy

Job Category: Other

-

EU work permit required: Yes

Job Reference:

8662617666420211712337154

Job Views:

3

Posted:

27.08.2025

Expiry Date:

11.10.2025

Job Description:

Evidilya, a 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, and close-out visits according to SOPs and study Monitoring Plan.
• Write Monitoring Reports and perform site management, 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 in Central-South Italy.

What We Offer:

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