Interest list
Clinical Research Coordinator
This is not an open job
We are not filling a seat here. This listing collects experts in this field so we can reach out when a client project needs them. Adding your name puts you on that list — it does not start a hiring process, and there is no vacancy behind it.
Rate set per project · Remote
Clinical TrialsGCP ComplianceData CollectionIRB Protocols
What this pays
Rates are set by the client project, not by us, and we do not know them until a contract is in place. Work is paid hourly or per task depending on the engagement. We would rather tell you that than publish a figure we cannot stand behind.
About the Role
Support AI training initiatives with clinical research expertise, protocol review, and structured data collection for healthcare AI tools.
Requirements
- Masters degree in clinical research, public health, or related field
- 2+ years experience coordinating clinical studies
- Working knowledge of GCP and IRB processes
- Detail-oriented with strong data skills
Responsibilities
- Review and annotate clinical trial documentation
- Validate AI-generated research protocol summaries
- Assist in structuring medical datasets for AI training
- Flag inconsistencies in clinical content