Clin Trials Research Associate
Position Qualifications:
Education Required
A Bachelor’s degree in health sciences or statistics or an equivalent combination of education and experience.
Experience Requirements
One to three years of work experience in clinical trial protocol management.
Demonstrated excellent written, verbal and interpersonal communication skills.
Demonstrated high attention to detail with strong organizational skills.
Knowledge of Institutional Review Board procedures, FDA regulations, GCP and study sponsor guidelines related to clinical trial research
Highly Desirable Qualifications
- Demonstrated knowledge of or experience with medical genetic and lysosomal storage disorders
- Experience with statistical analysis using SAS, R, and Microsoft Access
- CCRC (Certified Clinical Research Coordinator) or CCRP (Certified Clinical Research Professional) certification, OR a master’s degree in a related field (e.g. MPH)
- One to three years of experience in data entry and management
Desirable Qualifications
Knowledge of University policies, procedures and regulations
Experience processing expense reimbursements (e.g. travel, meals)
Willingness and ability to travel
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.
