Clinical Research Associate - freelance

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

Descrizione del lavoro

A leading Contract Research Organization is seeking a Clinical Research Associate to join their Operational team in Rimini. The role involves conducting site visits, managing data integrity, and requires a Bachelor's degree or MD. The ideal candidate will have proven experience in clinical monitoring and must hold CRA certification. This position offers a full remote job in a multicultural, dynamic environment.

Servizi

Full remote job

Multicultural work environment

Dynamic team

Competenze

• Bachelor’s degree/MD or equivalent in technical-scientific field.
• Proven experience in clinical monitoring with relevant training.
• Current CRA certification as per MoH decree 15/11/2011.

Mansioni

• Conduct and perform site visits, monitoring, and close-out visits.
• Write Monitoring Reports and manage site activities.
• Check data integrity and support the submission to ethics committees.

Conoscenze

Clinical monitoring experience

Organizational skills

Time management skills

MD or equivalent in technical-scientific field

GCP-ICH training

CRA certification

Formazione

Bachelor’s degree in technical-scientific field

Descrizione del lavoro

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Clinical Research Associate FREELANCE, Rimini

Client: Evidilya

Location:

Job Category:

Other

-

EU work permit required:

Yes

Job Reference:

8662617666420211712337130

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 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 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.