Clinical Trials Research Data Coordinator - Cancer Center

Required Qualifications

•          Bachelor’s degree or an equivalent combination of education and experience
•          6 to 12 months experience in a research or health care setting
•          Experience with medical terminology
•          Excellent verbal, written and interpersonal communication skills
•          Proficient in computer software applications
•          Ability to manage complex information with attention to detail and a high level of accuracy

Desirable Qualifications

•          Relevant experience in the conduct of clinical or laboratory research studies
•          Knowledge of regulatory guidelines and procedures
•          Clinical Research Coordinator Certification (SOCRA or ACRP)
•          Certification that allows for blood draw (Phlebotomy Technician, Certified Medical Assistant, LPN)
•          Experience conducting electrocardiograms (ECG)
•          Experience working with Epic
•          Experience working with OnCore Clinical Trials Management System
•          Knowledge of University of Iowa policies, procedures and regulations

Application Process: In order to be considered, applicants must upload a resume and cover letter(under submission relevant materials) that clearly address how they meet the listed required and desired qualifications of this position. 

Job openings are posted for a minimum of 14 calendar days. 

Successful candidates will be required to self-disclose any conviction history and will be subject to a criminal background check and credential/education verification.

References: Five professional references will be requested and required at a later step in the recruitment process

This position is not eligible for University sponsorship for employment authorization. 

With additional questions, please reach out to Sarah Waldschmidt at sarah-waldschmidt@uiowa.edu