Associate Clinical Research Coordinator
About The Position
This position will serve as an Associate Clinical Research Coordinator within the Department of Obstetrics and Gynecology, Division of Urogynecology. The Associate Clinical Research Coordinator is responsible for the execution of clinical research protocols, including leading efforts in gathering, compiling, and reporting data for a variety of research studies. This is a time-limited position with an estimated duration of 2 years, with potential for an extension. This is an in-person position at the UNC Urogynecology office in Raleigh. Ability to work in Raleigh, with potential travel to other UNC Health campuses for study-related activities, is a requirement of this position. This position is responsible for helping to support divisional research staff with the administration and management of multiple new and existing research projects in the Division of Urogynecology, which is located at the UNC Urogynecology office in Raleigh. The Associate Clinical Research Coordinator will be responsible for assisting in recruitment, scheduling, visit conduct, data collection, data entry, and monitoring. This position will be familiar with IRB process and with clinical research situations. The position will communicate clearly and effectively with primary investigators (PI) and be familiar with medical terminology. The position will adhere to standards of proper study conduct in compliance with the FDA Code of Federal Regulations and Good Clinical Practice. The position will inform and help the PIs with issues that arise during study execution, aid with preparation for monitoring or audits, and help with the collection of study results.
Requirements
- Familiarity with IRB process
- Familiarity with clinical research situations
- Ability to communicate clearly and effectively with primary investigators (PI)
- Familiarity with medical terminology
- Ability to work in Raleigh
- Potential travel to other UNC Health campuses for study-related activities
Responsibilities
- Execution of clinical research protocols
- Gathering, compiling, and reporting data for research studies
- Assisting in recruitment
- Scheduling
- Visit conduct
- Data collection
- Data entry
- Monitoring
- Communicating clearly and effectively with primary investigators (PI)
- Adhering to standards of proper study conduct in compliance with the FDA Code of Federal Regulations and Good Clinical Practice
- Informing and helping PIs with issues that arise during study execution
- Aiding with preparation for monitoring or audits
- Helping with the collection of study results
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
