Clinical Research Associate

1 giorno fa

Pavia PV, Provincia di Pavia; Lombardia, Italia Medpace Tempo pieno

Overview

In this CRA role at Medpace you will support the integrity of clinical studies across pharmaceutical and medical device development. You'll join a training-focused program (PACE) that accelerates your skills toward independent CRA responsibilities. You work across sites, regulators, and cross-functional teams to ensure compliant trials and data quality, with substantial travel. This position offers structured growth, exposure to multiple therapeutic areas, and a mission-driven environment that aims to improve patient outcomes. You'll be part of a supportive CRO with clear promotion paths and ongoing professional development.

Retribuzione / Benefits

  • Flexible work environment
  • Competitive compensation and benefits package
  • Competitive PTO packages
  • Structured career paths with opportunities for professional growth
  • Company-sponsored employee appreciation events
  • Employee health and wellness initiatives

Responsabilità

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites per protocol and SOPs
  • Communicate with site staff including coordinators and physicians
  • Verify investigator qualifications, training, resources, facilities, labs, equipment, and staff
  • Verify source documentation and maintain good documentation practices; handle protocol deviations
  • Ensure enrollment of eligible subjects and perform regulatory document reviews
  • Monitor adverse events and accurate data reporting per protocol
  • Assess site recruitment and retention and suggest improvements
  • Prepare monitoring reports and follow-up letters with significant findings and recommended actions

Requisiti fondamentali

  • Master degree in health-related field
  • Willingness to travel 60-80% nationally
  • Familiarity with Microsoft Office
  • CRA certification completed as per DMC 15/11/2011
  • Fluent in English and Italian
  • Strong communication and presentation skills a plus
  • strong communication
  • presentation skills
  • team collaboration
  • Microsoft Office
  • CRA certification
  • GCP and regulatory compliance knowledge