We are looking for a self-starter to join our team as a Clinical Research Coordinator. We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. As a CRC with this esteemed organization, you will be at the forefront of cutting-edge oncology research that can positively impact patient outcomes. Join us in our mission to advance medical knowledge and make a difference in the lives of patients in the Lone Tree, CO area and beyond.
We are looking for CRC's with over 1+ years of experience in clinical research.
RESPONSIBILITIES
1. Coordinates the implementation of multiple complex clinical research protocols.
2. Develops SOPs and templates with guidance from the PI and/or Clinical Research Manager.
3. Oversees and facilitates eligibility screening and study recruitment activities; implements strategies to increase accrual.
4. Manages sample processing, packing, and shipping according to protocol, applicable standards, and regulations.
5. Plans strategies to monitor, document, report, and follow-up on unanticipated occurrences
and protocol deviations. Develops and implements preventive/corrective actions.
6. Assumes leadership in protocol implementation and study progress, keeping investigators apprised of study progress.
7. Organizes/manages site visits and internal/external auditing activities as assigned.
8. Coordinates research team meetings; assures communications in cross functional teams.
9. Assures synchronization of study visits/procedures/ clinical tests with data collection schedules, established time- points; manages progress of study participants through protocol; expedites overall study progression.
10. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
BENEFITS
- Medical, Dental, Vision insurance
- PTO and paid holidays
- 401k with employer match
- Mental Health Assistance, Gym Discounts, Referral Program and more!
