Clinical Research Associate FREELANCE

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

Descrizione del lavoro

A CRO specializing in clinical trials is seeking a Freelance Clinical Research Associate to join their team in Torino. This role involves conducting site visits, writing monitoring reports, and ensuring data integrity while working in a multicultural environment. Candidates need a Bachelor's degree in a relevant field and proven experience in clinical monitoring. The position offers full remote work with travel required within Italy.

Servizi

Full remote work opportunity

Dynamic work environment

Competenze

• Proven experience in clinical monitoring and relevant training.
• Proven GCP-ICH training.
• Active CRA certification as per MoH decree 15/11/2011.

Mansioni

• Conduct SQV/Pre-study Visits and monitoring visits.
• Write monitoring reports and manage sites.
• Check data integrity.
• Support submissions to ethics committees.

Conoscenze

Clinical monitoring experience

Organizational skills

Time management skills

Formazione

Bachelor's degree/MD in a technical-scientific field

Descrizione del lavoro

Clinical Research Associate (Freelance) - Torino

Client:

Evidilya

Location:

Torino, Italy

Job Category:

Other

EU work permit required:

Yes

Job Reference:

866261766642021171233712

Job Views:

3

Posted:

27.08.2024

Expiry Date:

11.10.2024

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 (Freelance)

To reinforce the operational Italian team.

Main Responsibilities:

1. Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, and close-out visits according to SOPs and Study Monitoring Plan.
2. Write monitoring reports and perform site management, including follow-up activities.
3. Check data integrity.
4. Support the team in the submission of studies to ethics committees/IRBs.

Hard & Soft Skills:

1. Bachelor’s degree/MD or equivalent in a technical-scientific field.
2. Proven experience in clinical monitoring and relevant training in the field.
3. Proven GCP-ICH training.
4. Active CRA certification as per MoH decree 15/11/2011.
5. Excellent organizational and time management skills.

Additional Requirements:

• Availability to travel, especially within Central-South Italy.

What We Offer:

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