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 our esteemed organization, you will be at the forefront of cutting-edge endocrine 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 Chattanooga area and beyond.

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!