Freelance Clinical Research Associate (CRA) – Italy

Milan - Freelance (3 mois)

À propos de TempoPHARMA

For over 25 years, TempoPHARMA has been supporting talented professionals in the life sciences sector in their career development.

As specialists in healthcare recruitment and outsourcing, we work with leading organisations in clinical research, the pharmaceutical industry, biotechnology and medical devices.

Our approach is based on close collaboration, sector expertise and personalised support, enabling us to offer each candidate opportunities that match their ambitions.

Join us and contribute to the innovations that will shape the future of healthcare

Le poste

Clinact, a Contract Research Organization (CRO) specializing in clinical research, is looking for a Freelance Clinical Research Associate (CRA) based in Italy to support an international Phase IV cardiology study.

As part of the study close-out phase, you will be responsible for monitoring activities and the closure of 6 investigator sites in Italy.

Location: Italy
Contract: Freelance
Duration: Q4 2026
Workload: Approximately 40% (0.4 FTE)

Key Responsibilities

  • Conduct monitoring visits and oversee study activities at investigator sites.

  • Perform Source Data Verification (SDV) and Source Data Review (SDR), ensuring data accuracy and consistency with the EDC system.

  • Ensure compliance with the study protocol, ICH-GCP guidelines, and applicable Italian regulatory requirements.

  • Follow up on outstanding queries, missing data, and any identified discrepancies.

  • Review and maintain Investigator Site File (ISF) and Trial Master File (TMF) documentation, ensuring completeness and accuracy.

  • Coordinate and perform study close-out activities across 6 investigator sites in Italy.

Profil recherché

Profile

  • Degree in Life Sciences or a related scientific field.

  • Proven experience as a Clinical Research Associate, with strong expertise in clinical trial monitoring and site close-out activities.

  • Good knowledge of ICH-GCP guidelines and Italian clinical research regulations.

  • Fluency in Italian and professional proficiency in English.

  • Ability to work independently, with strong organizational skills and attention to detail.

  • Based in Italy and operating as a freelancer.

About Clinact

Clinact is a Contract Research Organization (CRO) specializing in clinical research. As part of the MultiHealth Group, Clinact provides expertise and support to pharmaceutical and healthcare companies throughout their clinical development projects.

Please send us your CV and availability, and our recruitment team will get in touch with you.

Détails sur le poste
Milan, Lombardie, Italie
Freelance (3 mois) - Temps partiel
Autres
Propulsé parTaleez