JOB SUMMARY
The clinical research coordinator will be responsible for managing and coordinating outpatient clinical trials.
EXPECTATIONS FOR ALL EMPLOYEES
Treat patients in a friendly, respectful, professional manner that exceeds our expectations. Reflects the mission statement of Advanced ENT and Allergy.
Job Responsibilities
- Submit financial documents and contracts to sponsors
- Submit regulatory documents for approval to study sponsors
- Prepare and submit documents for IRB approval
- Maintain communication with CRO/sponsor
- Maintain regulatory and study files
- Negotiate contract / budgets for clinical research studies
- Develop/customize informed consents
- Develop advertisements for upcoming and current trials
- Recruit patients for enrollment into trials
- Develop customized source documents for upcoming trials
- Be available for some travel to investigator meetings
- Perform study visits
- Maintain study drug accountability
- Maintain study supplies (drug, lab kits, CRF’s, etc.)
- Draw and process lab specimens to be sent to outside labs
- Consult with physician regarding abnormalities in physical findings or labs
- Consult with physician and sponsors regarding management of Adverse Events
- Complete Case Report Forms in a timely manner
- Be available for monitoring visits
- Be available during non-business hours if on-call physician or nurse has questions regarding a study
- Be available to cross-cover trials if another coordinator is out
- Be available for travel to office locations of Advanced ENT and Allergy and surgery centers to conduct study visits
Experience
Registered Nurse, Licensed Practice Nurse, or Licensed Healthcare Provide with research experience / CCRC preferred.
