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.
