Clinical Research Associate: Site Monitoring & Data Quality

IQVIA LLC

Milano

In loco

EUR 34.000 - 62.000

Tempo pieno

14 giorni+

Generatore di candidature

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Descrizione del lavoro

IQVIA LLC is seeking a Clinical Research Associate to monitor study sites and ensure data reported aligns with protocol and regulatory requirements. You will manage site communications, train staff, and track regulatory submissions, recruitment, and data queries.

Milano-based, onsite role requiring strong English communication and organized project oversight. Experience with GCP/ICH guidelines and CRA certification is essential; opportunity to contribute to global clinical research operations

Competenze

Master's degree in life sciences and CRA certification.
Completion of CRA training program or prior monitoring experience.
Good knowledge of GCP and ICH guidelines.
Strong written and spoken English.
Proficient in MS Word, Excel and PowerPoint.
Able to manage time and budgets and work with teams.

Mansioni

Perform site monitoring visits (selection, initiation, monitoring, close-out) per scope and regulatory requirements.
Drive and track subject recruitment plans to meet study needs.
Administer protocol training and maintain site communication.
Evaluate site practices for protocol conduct and compliance; escalate issues.
Track regulatory submissions, enrollment, CRF completion, data queries; support start-up if needed.
Maintain TMF/ISF and site documents; generate visit reports and follow-up letters.
Collaborate with study team for project execution; provide site management support.