Urology Associates - Denver
On-site · Denver, Colorado, United States
Job Summary
Clinical Research Coordinator for Urology Associates in Denver. Responsible for oversite of research projects, recruitment of studies, budget evaluation and negotiation, protocol evaluation and sponsor communication, regulatory compliance with FDA/GCP/ICH/federal and state regulations, obtaining patient consent, leadership in staff training and delegation, direct patient interactions including screening, history, exams and data collection (ECG, blood draw, vitals), EMR/eCRF data management, SOPs/NDAs/certifications maintenance, site visits and monitoring, budgeting, invoicing, and ensuring HIPAA/OSHA/CLIA compliance; requires knowledge of trial design and statistical methods, and ability to coordinate with IRB, PIs, Sub-Is, and sponsors.
Required Qualifications
- Minimum two (2) years of experience conducting clinical trials
- Proficiency in computer software to include Microsoft Office, EMR and Practice Management systems
- Certification by ACRP or an equivalent is preferred
- Ability to plan, schedule, prioritize and complete multiple tasks and demands is required
- Excellent oral and written communication, interpersonal, problem-solving and organizational skills are required
- Occasional overtime, evening and weekend work is required
- A valid driver’s license, dependable automobile and current auto insurance are required for occasional travel for business purposes and to work at satellite locations
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.