Contract Clinical Research Associate, Pain
We are actively seeking multiple contract Clinical Research Associates (CRAs) for an exciting opportunity supporting a global, quality-driven clinical trials Partner who has a strong, collaborative culture. The study is an acute pain trial (surgical and non-surgical) with multiple sites across FL, CA, TX, AZ, AR, and UT. This is a mixed remote and onsite monitoring role requiring approximately 50–75% travel, with a target start date of early to mid-August 2026 (FPI September 2026, database lock December 2026). We are seeking CRAs who have a minimum 5 years of recent experience as a fully dedicated regional/home-based field monitor for a CRO or pharma, at least 1 year of Pain study monitoring experience (acute pain a plus), a bachelor's degree from a North American institution, located in the SE, W, or SW US with no travel restrictions and proximity to a major airport, and at least 50% utilization availability (more work available if you would like to be fully dedicated). Apply below if this is you!
- Act as the "Site Manager" ensuring relationship with site(s) are positive, issues are resolved quickly, and communications are strong across all verticals.
- Assist with the development of study manuals, CRFs, monitoring standards, site study tools and other study materials as required.
- Develop and implement site recruitment, selection and initiation plan.
- Manage and drive patient recruitment and enrollment tracking.
- Provide training to sites on the study protocol, study conduct, CRF completion and data management expectations.
- Ensure essential document collection for completeness per regulatory requirements.
- Serve as a liaison with Investigators, Institutions and sites to provide support during the conduct of the clinical trial and serve as a resource for protocol and procedures.
- Demonstrate knowledge of on-site monitoring to ensure compliance with GCPs, study protocols, and SOPs.
Manage one or multiple studies. - Monitor product supplies/accountability including proper storage, dispensation, and disposal.
- Manage study completion activities including CRF collection, query resolution, record archiving and site closeout activities.
- Review in-house data and study tables.
- Mentor, coach and provide guidance to clinical staff as appropriate.
- Supervise and train other employees as appropriate.
- Minimum 5 years of experience as a fully dedicated regional/home-based field monitor for a CRO or pharma, with active experience within the last 2 years
- At least 1 year of Pain study monitoring experience (acute pain a plus); oncology and additional therapeutic area experience highly desirable
- Bachelor's degree from a North American institution
- Located in the Southeast, West, or Southwest US, with no travel restrictions and proximity to a major airport
- Minimum 50% utilization availability; up to 100% utilization available for those seeking a fuller workload
- Long-term contract
- Competitive pay rate