Job Summary
The Clinical Research Associate II position is based in Arizona, working predominantly onsite. This role is crucial for overseeing clinical trials, ensuring compliance with regulatory standards, and maintaining data integrity throughout the study process. The selected candidate will focus on enhancing patient safety during trials and will play a key role in collaborating with investigators and site personnel to facilitate the study execution.
Responsibilities
- Monitor clinical trials to ensure adherence to protocols and regulatory requirements.
- Manage site operations and maintain oversight of data integrity during the trials.
- Collaborate effectively with investigators and site staff to support study implementation.
- Review data meticulously to ensure accuracy and compliance with study requirements.
- Ensure patient safety is prioritized throughout the course of the trials.
Qualifications
- Previous experience in clinical trial monitoring, preferably within the oncology or pharmaceutical sectors.
- Strong understanding of clinical research regulations and guidelines.
- Excellent communication and interpersonal skills to foster collaboration with diverse teams.
- Ability to analyze and review clinical data for accuracy and adherence to standards.
- Proficiency in using clinical trial management systems and relevant software.
ICON 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.
