Clinical Research Associate
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* Flexible work environment
* Competitive compensation and benefits package
* Competitive PTO
* Structured career paths with growth
* Company-sponsored employee appreciation events
* Employee health and wellness initiatives Responsabilidades
* Conduct qualification, initiation, monitoring, and closeout visits per protocol
* Communicate with site staff including coordinators and investigators
* Verify investigator qualifications, training, resources, and facilities
* Verify data accuracy and ensure Good Documentation Practices; address protocol deviations per SOPs, GCP, and regulatory requirements
* Ensure enrollment of eligible subjects and perform regulatory document reviews
* Oversee medical device/investigational product/drug accountability
* Review adverse events and concomitant medications for accurate reporting
* Assess site recruitment/retention and suggest improvements
* Complete monitoring reports and follow-up letters with actionable recommendations to ensure compliance Requisitos principales
* University degree in a health or life science related field
* Minimum 1 year experience as Study Coordinator (SC), CRC, or CRA trainee
* Approximately 60-80% travel
* Proficient Microsoft Office and general computer literacy
* Outstanding communication and presentation skills
* Detail-oriented with good time management
* Excellent verbal and written communication in English and Spanish
* Catalan language fluency is a plus
* strong communication
* attention to detail
* time management
* Microsoft Office
* Good Documentation Practices (GDP)
* GCP compliance
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