Clinical Research Coordinator
- New Sponsor Relations
- New protocol specialist
- CTA (clinical trial agreements) and Budget
- PSSV, PSV, SIV (visits to get clinical trials started and approved)
- Invoicing and reconciliation
- Certified Clinical Research Coordinator preferred, but not required
- Maintenance of SOP and Training of SOP (standard operating procedures)
- Training new staff
- Coordinator of clinical research for patients with neurological disorders
- Orchestration of patient screening, consent, enrollment, and follow-up
- Draw, collect, and process biological specimens
- Manage study data and regulatory documents
- Administer scales as required per protocol
- Manage registries and observational studies involving neurological disorders
- Administrator for study start-up, IRB submissions, budget and contract negotiations, budget drafting, and accounting/reconciliation
- Supervision of monitoring visits, audits, data management, and study close out
Compensation dependent on experience.
Job Type: Full-time
Pay: $27.00 - $30.00 per hour
Benefits:
Education:
Work Location: Hybrid remote in Basalt, CO 81621
