Pediatric Hematology/Hemostasis Research Assistant

University of Iowa; Iowa City (IA); On-site; USD 42,000 - 56,000; Full time

Job summary

The University of Iowa’s Stead Family Department of Pediatrics is seeking a Clinical Research Assistant in Pediatric Hematology/Hematostasis to support multiple studies focused on bleeding and clotting disorders. You will coordinate regulatory activities, recruit and enroll participants, and manage data collection and quality assurance under supervision.

Responsibilities include designing data forms, coordinating visits, and communicating with investigators, patients, and families to ensure

Qualifications

• Bachelor’s degree in a health science related field.
• Proven ability to utilize medical terminology.
• Excellent organizational and time‑management skills.
• Excellent written and verbal communication skills.
• Proficient in computer software applications including spreadsheet and database experience.
• Experience coordinating multiple projects and multiple functions independently.
• Knowledge of regulations that apply to human research.

Responsibilities

• Coordinate data management activities for research studies.
• Design data collection tools and forms for participants, procedures, and samples.
• Screen, recruit, enroll, and obtain informed consent.
• Schedule visits and coordinate study procedures per protocol.
• Maintain and verify clinical research data with quality assurance.
• Prepare regulatory documents and regulatory communications.
• Serve as liaison among participants, healthcare providers, sponsors, and sites.
• Assist with budget development and provide staff mentorship.

Skills

Medical terminology

Organization

Communication

Computer skills

Project coordination

Regulatory knowledge

Education

Bachelor's degree in a health science related field

Tools

Spreadsheet software

Database software

Job description

The University of Iowa’s Stead Family Department of Pediatrics is seeking a Clinical Research Assistant in Pediatric Hematology/Hematostasis to support multiple studies focused on bleeding and clotting disorders. You will coordinate regulatory activities, recruit and enroll participants, and manage data collection and quality assurance under supervision.

Responsibilities include designing data forms, coordinating visits, and communicating with investigators, patients, and families to ensure