IQVIA is looking to solve the problem of conducting clinical trial activities in accordance with all applicable regulations to support groundbreaking studies and improved patient outcomes.
Requirements
- Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
- Clinical Research Coordinator experience within a similar setting
- Clinical skills experience including obtaining vitals, phlebotomy, EKG, etc.
- Knowledge and experience of site operations and the drug development process
- Computer proficiency in use of Microsoft Word, Excel
Responsibilities
- Coordinates as primary CRC 1-3 studies on average of low to medium complexity, with oversight by a manager or higher-level CRC.
- Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
- Obtains informed consent of research subjects
- Collects patient/research participant history
- Collects and maintains source documentation
- Manages inventory and administers test articles/investigational product to participants
- Performs data entry and query resolution
Other
- Ability to work on-site at the site in Kansas City, MO
- Ability to travel to other clinic locations, within the area, when needs arise
- Effective communication
- Strong interpersonal and team building skills
- Bachelor's degree or equivalent experience
