Clinical Research Coordinator I

Tekton Research Inc • Longmont, CO

3h

About The Position

The CRC I is part of a collaborative site team. Projects will include training on the responsibilities of clinical trials, while also being responsible for the daily operations and overall management of assigned clinical trials as deemed appropriate by site management based on training and experience. It is the responsibility of the CRC I to communicate with site staff, management, and study participants. Adherence to Tekton SOPs is required.

Requirements

• 6 months - 2 yrs Clinical Research experience preferred
• Phlebotomy required
• Self-motivated, team player with strong attention to detail & ability to multitask
• Ability to read, write, and speak English language
• Ability to work independently and as a team member
• Potential for travel to assist & train at Tekton Research sites
• Knowledge of basic medical terminology
• GED or HS Diploma required, advanced training or some college preferred

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED