Clinical Research Associate II — Hybrid & Impactful Role

CTI Clinical Trial and Consulting Services; Torino; Hybride; EUR 42 000 - 60 000; Plein temps

Résumé du poste

CTI Clinical Trial and Consulting Services is seeking a CRA to act as the main CTI contact for assigned study sites and to conduct site visits (PSV, SIV, IMV, COV) while ensuring quality and regulatory compliance. You will support study start-up activities, feasibility assessments, and site selection, collecting essential regulatory documents and participating in team meetings.

The role requires 3–5 years of clinical research experience as a CRA or related field, a life science background, and

Qualifications

• Must have 3–5 years of clinical research experience as a CRA or related role.
• Background in life sciences or related field is required.
• Strong knowledge of ICH-GCP and regulatory requirements.

Responsabilités

• Serve as main CTI contact for assigned study sites and ensure regulatory compliance.
• Conduct site visits (PSV, SIV, IMV, COV) and complete deliverables on time.
• Assist with or oversee start-up activities, feasibility, and site selection.

Connaissances

CRA experience

Life science background

ICH-GCP knowledge

English (B2)

Description du poste

CTI Clinical Trial and Consulting Services is seeking a CRA to act as the main CTI contact for assigned study sites and to conduct site visits (PSV, SIV, IMV, COV) while ensuring quality and regulatory compliance. You will support study start-up activities, feasibility assessments, and site selection, collecting essential regulatory documents and participating in team meetings.

The role requires 3–5 years of clinical research experience as a CRA or related field, a life science background, and