Job Summary
Fortrea is in search of a Clinical Research Associate II with specialized knowledge in Phase I trials to facilitate site monitoring, maintain study documentation, guarantee adherence to protocols, and ensure the accuracy of data for clinical studies. This position is based in Daytona Beach, Florida, and entails regular travel to various sites.
Responsibilities
- Conduct monitoring visits at clinical trial sites to evaluate compliance with study protocols.
- Manage and maintain study files, ensuring all necessary documentation is organized and up-to-date.
- Oversee the integrity of data collected during clinical trials.
- Communicate effectively with site personnel regarding study requirements.
- Provide support and guidance to investigators and site staff throughout the study process.
Qualifications
- Proven experience as a Clinical Research Associate, particularly in Phase I trials.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent organizational and communication skills.
- Able to travel frequently to clinical sites as required.
- Detail-oriented approach to managing clinical data and study documentation.
Fortrea provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
