What are the responsibilities and job description for the Clin Trials Research Associate - ICTS Coordinator Core position at Jobs@UIOWA?
The clinical trial research associate/ data manager will be an integral member of the research team in the Institute for Clinical and Translational Science and the Department of Family Medicine. This position will provide support for these departments by performing activities which are vitally important to establish the research core for the department, as well as to grow and foster innovation through research support endeavors. The clinical trial research associate/ data manager will apply clinical skills to administer, deliver, and evaluate research protocols.
Duties to include but not limited to:
- Perform clinical/health care research activities in the Department of Family Medicine.
- Monitor the our site participating in a PCORI Study, which is a large multi-site clinical trial.
- Collaborate with Principal Investigator and the study team in the development, execution, administration and maintenance of protocols and clinical studies and provide input into descriptions of complex research procedures.
- Assess participants for problems related to protocol.
- Participate in the design; development and testing of clinical research trial data systems.
- Maintain communication between health care clinical information systems and research data systems.
- Manage and organize regulatory documentation.
- Prepare and submit regulatory documents.
- Participate in preparation of grant applications for extramural funding.
- Assist with tracking and reconciling grant/trial budget free balances and identify opportunities to ensure that grant funding is being used as intended and awarded.
Pay Grade: 4A
https://hr.uiowa.edu/pay/guide-pay-plans
-Fringe benefit package including paid vacation; sick leave; health, dental, life and disability insurance options; and generous employer contributions into retirement plans
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Required Qualifications
- A Bachelor’s degree in a Health Science field or an equivalent combination of education and research experience is required.
- Working knowledge of Good Clinical Practice (GCP) in research.
- Excellent written and verbal communication skills.
- Ability to work nights and weekends is required.
- A minimum one year of clinical research experience.
- Proficiency in Microsoft Word, Outlook, and Excel.
- The ability to travel between multiple clinical trial sites.
- A valid driver’s license and the ability to meet and maintain University Driving Policy standards.
· Previous experience writing manuscripts for publication.
· Experience with REDCap, Epic, ICart, and ACCESS.
· Previous experience in data collection and entry.
· Experience in processing research regulatory documents.
· A current license to practice nursing in Iowa by the time of hire.
· The ability to work independently.
· Excellent time management skills and ability to perform detail-oriented work.
Application Process:
In order to be considered for an interview, applicants must upload the following documents and mark them as a “Relevant File” to the submission:
Remote within Iowa: This position is eligible for primarily remote work but may require limited work onsite at times. Remote work must be performed at a location within the state of Iowa and comply with the remote work program and related policies.
As previously discussed, this position is eligible for hybrid work within Iowa and will require a work arrangement form to be completed upon the start of your employment. Per policy, work arrangements will be reviewed annually, and must comply with the remote work program and related policies and employee travel policy when working at a remote location.
