Senior Clinical Research Associate - 0.2 Fte - Italy

ProPharma

Italy
Hybrid
Clinical monitoring for assigned protocols
Ensuring gcp and regulatory compliance
Data review, query generation and resolution
ProPharma is seeking a Senior Clinical Research Associate (CRA) for a part-time (0.1 - 0.2 FTE) contract role in Italy, focusing on clinical monitoring for various protocols and investigational sites. The candidate should have at least 2 years of CRA experience and knowledge of regulatory guidelines, with flexibility to work in a hybrid environment

Job Summary

  • ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.
  • The Clinical Research Associate (CRA) is responsible for clinical monitoring for assigned protocols and investigational sites.
  • We celebrate our differences and strive to create a workplace where each person can be their authentic self.

Matching Summary

Match Score: 85

ProPharma is seeking a Senior Clinical Research Associate (CRA) for a part-time (0.1 - 0.2 FTE) contract role in Italy, focusing on clinical monitoring for various protocols and investigational sites. The candidate should have at least 2 years of CRA experience and knowledge of regulatory guidelines, with flexibility to work in a hybrid environment.

Skills & Requirements

Must-have

  • Clinical monitoring for assigned protocols
  • Ensuring GCP and regulatory compliance
  • Data review, query generation and resolution
  • Travel to study sites
  • Electronic data capture (EDC) experience

Nice-to-have

  • Rare disease experience
  • Pediatric experience
  • Training site staff on study requirements
  • Reviewing time sheets and expense reports

Key Requirements

  • 2+ years of experience as a Clinical Research Associate
  • Bachelor's degree or equivalent combination of education and experience
  • Knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs

Work Rights

Not specified

Tailored Resume

Cover Letter