Clinical Research Assistant (Full-Time/Contractual C1)

Primary Duties

• Assisting with the performance of research projects in a clinical setting, including screening and recruitment of potential study subjects and collection and organization of data.
• Assist with data collection by conducting research interviews, reviewing medical charts, and accessing computerized medical information systems.
• Aid in the development, submission, and provision of content for grants, papers, abstracts, manuscripts, and presentations.
• Support the Principal Investigator (PI) and other research staff in the development of research protocols and materials.
• Perform administrative duties, maintaining communication with participants and colleagues regarding protocol-specific information and research orders.
• May also assist with providing assessments and ensuring protocol compliance while participants are in a study.

Minimum Qualifications

• Education: Bachelor’s degree in a scientific field of study related to the research of the clinical setting.
• Experience: May consider a combination of directly related experience and education.

Knowledge, Skills, And Abilities

• Knowledge of position requirements.
• Knowledge of all applicable requirements, regulations, and laws.
• Skill in the effective use of applicable technology/systems.
• Ability to effectively communicate both verbally and written thoughts, ideas, and facts.
• Ability to work cooperatively with others and independently.
• Ability to demonstrate, understand, apply, and adhere to the UMB Core Values of Respect and Integrity, Well-being and Sustainability, Equity and Justice, and Innovation and Discovery.

Hiring Range

$45,000 - $48,500 per year / Commensurate with education and experience