About this role
Own Your Studies. Grow Your Career.
If you’re ready to step into real ownership of clinical trial coordination – managing your own studies, leading patient visits, and working with the independence that comes from having built a strong foundation – this role is the next step.
As a Clinical Research Coordinator I at Profound Research, you’ll serve as the primary coordinator for assigned studies at one of our sites. You’ll manage study activities from start-up through closeout, lead interactions with study participants, maintain audit-ready documentation, and work directly with investigators, sponsors, and CROs. This isn’t a support role – you own your studies, and your work directly impacts patient safety, data integrity, and trial outcomes.
What You’ll Do
Serve as primary coordinator for assigned clinical trials, managing study activities from start-up through closeout
Physical Requirements & Work Environment
This role is performed on-site at a clinical or office facility and requires prolonged periods of sitting, standing, or walking throughout the work environment
Requires the ability to communicate clearly in verbal and written forms and to read and interpret detailed materials
Must be able to navigate a clinical facility, including areas with limited space, and transport supplies or work materials as needed
May be required to wear personal protective equipment (PPE) in accordance with facility protocols
Travel between company sites, meetings, or partner locations may be required
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role
Why Join Profound Research?