Clinical Research Associate - freelance

JR Italy; Lecce; In loco; EUR 40.000 - 60.000; Tempo pieno

Descrizione del lavoro

A global clinical research organization is seeking a Clinical Research Associate to support its operations in Lecce, Italy. The role involves conducting site visits, ensuring data integrity, and managing site activities. Candidates should have a degree in a technical field and relevant clinical monitoring experience. The position offers a full remote work opportunity within a dynamic and multicultural environment.

Servizi

Full remote work opportunity

Dynamic work environment

Competenze

• Experience in clinical monitoring and relevant training.
• GCP-ICH training certification required.
• Active CRA certification per MoH decree.

Mansioni

• Conduct SQV/Pre-study Visits and site initiation visits.
• Write Monitoring Reports and manage site activities.
• Ensure data integrity and assist submissions to ethics committees.

Conoscenze

Clinical monitoring

Organizational skills

Time management

Data integrity assurance

Formazione

Bachelor’s degree, MD or equivalent

Descrizione del lavoro

Clinical Research Associate (Freelance) - Lecce

Client:

Evidilya

Location:

Lecce, Italy

Job Category:

Other

EU work permit required:

Yes

Job Reference:

8662617666420211712337152

Job Views:

3

Posted:

27.08.2025

Expiry Date:

11.10.2025

Job Description:

Evidilya, a dedicated Contract Research Organization of Sprim Health Group, operates as a full-service international company specializing in observational, pre-clinical, and clinical trials. We are seeking a:

Clinical Research Associate

to support the Italian operational team.

Main Responsibilities:

• Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, and close-out visits according to SOPs and study Monitoring Plan.
• Write Monitoring Reports and manage site activities, including follow-up activities.
• Ensure data integrity.
• Assist in the submission of studies to ethics committees/IRBs.

Required Skills and Qualifications:

• Bachelor’s degree, MD, or equivalent in a technical-scientific field.
• Experience in clinical monitoring and relevant training in the field.
• GCP-ICH training certification.
• Active CRA certification as per MoH decree 15/11/2011.
• 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.