Clinical Research Associate - freelance

JR Italy; Milano; 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 operational Italian team. Responsibilities include conducting site visits, writing monitoring reports, and ensuring data integrity. Candidates should have a relevant degree, CRA certification, and experience in clinical monitoring. This role offers a full remote work environment and a multicultural team.

Servizi

Multicultural, young, and dynamic work environment

Full remote job

Competenze

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

Mansioni

• Conduct SQV/Pre-study Visits and site initiation visits.
• Write Monitoring Reports and perform site management.
• Check data integrity.

Conoscenze

Clinical monitoring

Organizational skills

Time management

Formazione

Bachelor’s degree/MD or equivalent

Descrizione del lavoro

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Clinical Research Associate FREELANCE, Milano

Client: Evidilya

Location:

Job Category: Other

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EU work permit required: Yes

Job Reference:

866261766642021171233710

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 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, close out visits, according to SOPs and study Monitoring Plan
• Write Monitoring Reports and perform 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
• Proven experience in clinical monitoring and 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