Clinical Research Associate - freelance

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

Descrizione del lavoro

An international Contract Research Organization is seeking a Clinical Research Associate to join their team in Latina, Italy. This full remote position involves conducting clinical trial monitoring visits, writing reports, and ensuring data integrity. The ideal candidate holds a Bachelor's degree in a relevant field and has proven experience in clinical monitoring. The role requires availability to travel within Central-South Italy and offers a multicultural work environment.

Servizi

Full remote job

Multicultural, young and dynamic work environment

Competenze

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

Mansioni

• Conduct SQV/Pre-study Visits, site initiation visits and monitoring visits.
• Write Monitoring Reports and perform site management.
• Support submission of the study to ethics committees/IRBs.

Conoscenze

Clinical monitoring

Organizational skills

Time management

Formazione

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

Strumenti

GCP-ICH training

Descrizione del lavoro

Social network you want to login/join with:

Clinical Research Associate FREELANCE, latina

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Client:

Evidilya

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

8662617666420211712337153

Job Views:

3

Posted:

27.08.2025

Expiry Date:

11.10.2025

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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, is 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 performing 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
• Proved experience in clinical monitoring and proven 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