Clin Trials Rsrch Associate
Required Qualifications
A Bachelor’s degree or an equivalent combination of education and experience is required.
1 year of related experience including experience with preparation of IRB submissions or regulatory submissions and participation in clinical trials research is required.
Excellent time management skills and the ability to perform detail orientated work independently is required.
Excellent written and verbal communication skills are required.
Proficiency in computer software and database applications (MS Word, Excel, Outlook, PowerPoint, Research databases such as RedCap)
Desirable Qualifications
Experience with following specific protocol techniques and management is desirable.
Previous involvement in clinical research is desirable.
Experience working in an academic research institution is desirable.
Knowledge of urology and cancer research is desirable.
Application Process: In order to be considered, applicants must upload a resume, cover letter options (under submission relevant materials) that clearly address how they meet the listed required and desired qualifications of this position.
Equal opportunity/affirmative action employer
The University of Iowa is an equal opportunity/affirmative action employer. All qualified applicants are encouraged to apply and will receive consideration for employment free from discrimination on the basis of race, creed, color, religion, national origin, age, sex, pregnancy (including childbirth and related conditions), disability, genetic information, status as a U.S. veteran, service in the U.S. military, sexual orientation, gender identity, or associational preferences.
Persons with disabilities who need assistance or accommodations with the application or interview process may contact University Human Resources/Faculty and Staff Disability Services, (319) 335-2660 or fsds@uiowa.edu. For jobs in UI Health care, please contact UI Health care Leave & Disability Administration at 319-356-7543.
