Clinical Research Associate FREELANCE

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

Descrizione del lavoro

An international Contract Research Organization is seeking a Clinical Research Associate in Cagliari, Italy. The successful candidate will be responsible for conducting visits, monitoring data integrity, and ensuring compliance with SOPs. A Bachelor's degree or MD in a technical-scientific field and clinical monitoring experience are essential. The role offers a full remote work opportunity within a multicultural and dynamic environment.

Servizi

Full remote job

Dynamic work environment

Multicultural team

Competenze

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

Mansioni

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

Conoscenze

Clinical monitoring experience

GCP-ICH training

Time management skills

Organizational skills

Formazione

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

Descrizione del lavoro

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Clinical Research Associate FREELANCE, Cagliari

Client: Evidilya

Location: Cagliari, Italy

Job Category: Other

EU work permit required: Yes

Job Reference:

8662617666420211712337142

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 in the submission of 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 job.
• Multicultural, young, and dynamic work environment.