Clinical Research Associate
16 ore fa
Varese, Lombardia, Italia
Medpace
Tempo pieno
Gratuito con email o Google
Salva questo lavoro e mantieni la tua ricerca organizzata
Crea un account gratuito per salvare lavori, creare avvisi e tornare a questa inserzione dalla tua dashboard.
Gratuito con email o Google
Continuando accetti i nostri Termini & Informativa sulla privacy.
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
* 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