Clinical Trials Research Assistant - Pediatrics Neurology
University of Iowa · Iowa City, IA · 2 days ago
AnalystFull-time
Duties
- Read and understand complex protocols.
- Discuss protocols with potential study participants either in person or over the phone.
- Educate patients and families on scope of study, potential risks and benefits, possible alternatives, and study requirements for patient.
- Screen for subject eligibility and obtain informed consent for clinical trials/studies.
- Schedule patient visits within parameters specified in study protocol.
- Schedule trial-related procedures and visits.
- Meet with patients during study visits.
- Perform or assist with patient assessments and review of medical history.
- Absorb and enter clinical research data in a timely manner.
- Absorb and maintain regulatory documents from subjects and assist in preparation of required regulatory forms and documentation according to protocol.
- Absorb and resolve monitoring visit issues.
- Report any reportable events to appropriate party.
- Absorb and maintain compliance of regulatory guidelines and proper maintenance of documents.
- Absorb and assist in budget development and monitoring for study.
Education Requirement
Bachelor's degree in health sciences or a related field or an equivalent combination of education and experience.
Experience Requirements
- 1-2 years previous research experience.
- Proficient with Microsoft Office programs (Word, Excel, PowerPoint).
- Previous experience working with pediatric patients & their families.
- Excellent written and verbal communication and interpersonal skills.
- Demonstrated high attention to detail with strong organizational skills.
Highly Desired Qualifications
- Ability to work in a fast-paced and dynamic environment.
- Clinical research experience.
- Capable of working independently.