Clinical Research Associate FREELANCE

JR Italy; Prato; In loco; EUR 30.000 - 50.000; Part-time

Descrizione del lavoro

A leading CRO is seeking a Clinical Research Associate to join their Italian team in Prato. This remote role requires monitoring clinical trials, ensuring data integrity, and supporting submissions to ethics committees. Candidates must have a relevant degree, prior clinical monitoring experience, and current CRA certification. The team offers a multicultural and dynamic work environment with opportunities for travel, particularly in Central and South Italy.

Servizi

Full remote work opportunity

Multicultural, young, and dynamic work environment

Competenze

• 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.

Mansioni

• Conduct pre-study, monitoring, and close-out visits according to SOPs.
• Write Monitoring Reports and perform site management including follow-ups.
• Support the submission of the study to ethics committees/IRBs.

Conoscenze

Clinical monitoring

Data integrity

Organizational skills

Time management

Technical-scientific knowledge

Formazione

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

Descrizione del lavoro

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Clinical Research Associate FREELANCE, Prato

Client:

Evidilya

Location:

Prato, Italy

Job Category:

Other

EU work permit required:

Yes

Job Reference:

8662617666420211712337140

Job Views:

3

Posted:

27.08.2023

Expiry Date:

11.10.2023

Job Description:

Evidilya, the dedicated Contract Research Organization of Sprim Health Group, operates as a full-service international organization specializing 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, and close-out visits according to SOPs and the study Monitoring Plan.
• Write Monitoring Reports and perform site management, including 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 and South Italy.

What we offer:

• Full remote work opportunity.
• Multicultural, young, and dynamic work environment.