Job Summary
Fortrea is on the lookout for a Clinical Research Associate 2 with a specialization in oncology to oversee clinical trial sites within the Las Vegas region. This role necessitates approximately 8-10 days of on-site engagement each month, focusing on monitoring operations, ensuring data accuracy, and managing site activities across a range of studies.
Responsibilities
- Conduct monitoring visits to clinical trial sites, ensuring adherence to protocols.
- Perform data integrity assessments to confirm the reliability of collected information.
- Facilitate site management tasks to support the smooth progression of clinical studies.
- Collaborate with site staff and participate in training sessions as needed.
- Document and report on the findings from monitoring visits.
Qualifications
- Prior experience in oncology clinical research roles is essential.
- A strong understanding of clinical trial regulations and Good Clinical Practice (GCP).
- Excellent communication skills for effective interactions with clinical site personnel.
- Ability to work independently while managing multiple responsibilities in a timely manner.
- Proficiency in data management and analysis relevant to clinical trials.
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.
