Clinical Research Associate FREELANCE

JR Italy; Roma; In loco; EUR 35.000 - 50.000; Tempo pieno

Descrizione del lavoro

A clinical research organization is seeking a Clinical Research Associate to join their team in Roma. This full-remote position includes responsibilities such as conducting site visits, ensuring data integrity, and managing submissions to ethics committees. Candidates must have a Bachelor’s degree in a related field and valid CRA certification. The role offers a dynamic, multicultural work environment and requires availability for travel, particularly in Central-South Italy.

Servizi

Full remote job

Multicultural, young, and dynamic work environment

Competenze

• Bachelor’s degree/MD or equivalent required.
• Proven experience in clinical monitoring is necessary.
• Active CRA certification as per MoH decree is essential.

Mansioni

• Conduct SQV/Pre-study visits and site management.
• Write monitoring reports and manage follow-up activities.
• Support submissions to ethics committees/IRBs.

Conoscenze

Clinical Monitoring

Data Integrity

Organizational Skills

Time Management

GCP-ICH Training

Formazione

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

Descrizione del lavoro

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Clinical Research Associate FREELANCE, Roma

Client: Evidilya

Location: Roma

Job Category: Other

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EU work permit required: Yes

Job Reference:

866261766642021171233711

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 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 perform site management, addressing follow-up 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 training in the field.
• Proven GCP-ICH training.
• Active 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.