Clin Trials Rsrch Asst/Data Mg - ICTS Coordinator Core
About The Position
The clinical trial research assistant/ data manager will be an integral member of the research team in the Institute for Clinical and Translational Science (ICTS) Coordinator Core. This position will provide research support by performing activities which are vitally important to establish the research core for the ICTS, as well as to grow and foster innovation through research support endeavors. The clinical trial research assistant/ data manager will apply clinical skills to administer, deliver, and evaluate research protocols. About ICTS: The Institute for Clinical and Translational Science (ICTS) at the University of Iowa was approved by the Iowa Board of Regents in 2007 to support the work of investigators involved in clinical and translational science. Our mission is to accelerate translational science through programs to develop the translational workforce, to promote engagement of community members and other stakeholders, to promote research integration across the lifespan, and to catalyze innovative clinical and translational research. These efforts will lead to the development of novel therapies and healthcare delivery strategies, the integration of translational research and clinical practice, and, ultimately to measurable improvements in the health of Iowa and the nation.
Requirements
- A Bachelor’s degree in a Health Science field or an equivalent combination of education and research experience.
- Excellent written and verbal communication skills.
- Working knowledge of Good Clinical Practice (GCP) in research.
- Ability to work nights and weekends.
- Proficiency in Microsoft Word, Outlook and Excel.
Nice To Haves
- Basic (6 months - 1 year) of clinical research experience.
- Educational background in public health or experience participating in public health research projects.
- Previous experience writing manuscripts for publication.
- Experience with REDCap, Epic, ICart, I-CTMS, and ACCESS.
- Previous experience in data collection and entry.
- Experience in processing research regulatory documents.
- The ability to work independently.
- Excellent time management skills and ability to perform detail-oriented work.
Responsibilities
- Perform clinical/health care research activities in various departments.
- Screen, recruit, enroll and obtain informed consent for clinical research activities.
- Assist in the design, development, execution, administration and maintenance of protocols and clinical studies and provide input into descriptions of complex research procedures.
- Assist patients with problems related to protocol.
- Assist in the design, development, execution, administration and maintenance of protocols and clinical studies and provide input into descriptions of complex research procedures.
- Assist patients with problems related to protocol.
- Manage and organize regulatory documentation.
- Prepare regulatory submissions.
- Conduct literature reviews and maintain citation database.
- Pull data reports from qualitative data management software.
- Participate in preparation of grant applications for extramural funding.
- Provide assistance with tracking and reconciling grant/trial budget free balances and identify opportunities to ensure that grant funding is being used as intended and awarded.
Benefits
- 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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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
