Clinical Research Associate (CRA)
VitaliefPhoenix, Arizona, United States
Posted October 15, 2025
Part Time
About the Company
Vitalief Inc. specializes in recruiting top talent for clinical trials, offering strategic partnerships to overcome workforce challenges. By investing in their team and delivering high-quality services, Vitalief ensures clients can adapt to the evolving needs of the industry, ultimately making a positive impact on patients' lives.
Job Description
Vitalief is seeking a skilled Clinical Research Associate (CRA) to support pharmaceutical clients in executing clinical trials. The role combines CRO oversight with hands-on monitoring activities, contributing both strategically and operationally within a dynamic biotech environment. This is a hybrid position with potential for remote work once on-site becomes essential.
Requirements
- Support concurrent trials through proactive coordination and oversight.
- Conduct remote and on-site monitoring visits, including qualification, initiation, interim, and closeout activities.
- Perform Source Document Verification (SDV) and ensure data accuracy, completeness, and protocol compliance.
- Review clinical documentation (e.g., CRFs, monitoring plans, data management plans) for quality and consistency.
