Job Summary
Fortrea is in search of a Clinical Research Associate 2 based in the Denver, Colorado region, focusing on oncology clinical studies. The ideal candidate will possess a minimum of two years of monitoring experience and will be responsible for overseeing trial sites to ensure adherence to regulations and integrity of data.
Responsibilities
- Conduct site monitoring visits to ensure compliance with clinical trial protocols and regulatory requirements.
- Verify the integrity of data collected during the clinical trials.
- Facilitate effective communication between study sites and the sponsor.
- Document any findings and ensure timely resolution of issues identified during site visits.
Qualifications
- A minimum of two years of experience in clinical monitoring, specifically in oncology trials.
- Strong understanding of GCP (Good Clinical Practice) and regulatory guidelines.
- Excellent communication and interpersonal skills to effectively interact with site personnel.
- Ability to work both onsite and remotely, adapting to the needs of the trial and the team.
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.
