Temporary Clinical Sciences Professional
About The Position
This Clinical Sciences Professional works in the CU Nursing Office of Research and Scholarship. Its responsibilities include supporting the principal investigator in their study to conduct a randomized controlled study evaluating a technology-supported physical activity coaching program. The position is responsible for screening and recruiting study participants at all stages, performing data collection and entry, tracking study progress, and preparing reports for weekly study team meetings. This description is a summary only and describes the general level of work being performed, it is not intended to be all-inclusive. The duties of this position may change from time to time and/or based on business need. We reserve the right to add or delete duties and responsibilities at the discretion of the supervisor and/or hiring authority.
Requirements
- Bachelor’s degree in any field
- Knowledge and understanding of federal regulations and Good Clinical Practice (GCP)
- Ability to communicate effectively, both in writing and orally
- Ability to establish and maintain effective working relationships with employees at all levels throughout the institution
- Outstanding customer service skills
- Outstanding organizational skills and attention to detail
- Ability to represent the University in a professional and positive manner
- Ability to collaborate as a member of a team and to work highly independently to meet competing demands.
- Innovative problem-solving skills, and ability to thrive on challenges encountered in fluid, complex environment
- Knowledge of institutional and governmental research administration policies and procedures and ability to strictly follow IRB, FDA, and HIPAA regulations.
- Excellent project management, organizational, and time management skills.
- Fundamental knowledge of clinical research.
- Enthusiasm for and experience in collaborative team environment
Nice To Haves
- Experience participating in clinical studies
- Experience reviewing Epic (EHR) data
- Experience recruiting study participants
Responsibilities
- Review Epic (EHR) and screen study participants
- Recruit study participants via patient portal, phone, and email
- Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support
- Enter and collect data obtained from research in an accurate and timely manner
- Adhere to research regulatory standards
- Maintain detailed records of studies to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures and other regulatory guidelines
Benefits
- Temporary employees are only eligible for sick leave benefits.
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What This Job Offers
Career Level
Entry Level
