Job Summary
The role of Clinical Research Associate II involves providing support for oncology clinical trials within a sponsor-focused setting. You will be the main contact point between investigational sites and the sponsor, ensuring effective communication and coordination throughout the research process.
Responsibilities
- Facilitate site visits to monitor clinical trials.
- Act as the primary connection between the investigational sites and the sponsoring organization.
- Ensure compliance with study protocols and regulatory requirements.
- Assist in the management of trial data and documentation.
Qualifications
- A Bachelor’s degree in Life Sciences or an RN qualification is required.
- A minimum of 2 years of experience working on-site in clinical research is essential.
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.
