Clinical Research Assistant – Data, IRB & Grants

University of Maryland, Baltimore; Baltimore (MD); On-site; USD 50,000 - 70,000; Full time

Job summary

The University of Maryland, Baltimore (UMB) is seeking a detail-oriented researcher to support clinical studies in a professional setting. Responsibilities include recruiting subjects, collecting and organizing data, reviewing medical records, and ensuring protocol compliance.

The role requires independent judgment and collaboration with the research team to advance study objectives. Qualifications include a Bachelor’s degree in a scientific field and preferred clinical research experience.

Qualifications

• Bachelor's degree in a scientific field related to clinical research.
• Prior clinical research experience preferred.
• Additional related education or experience may substitute for the degree/experience requirement.

Responsibilities

• Assist with recruiting of potential study subjects and collection/organization of data.
• Assist with data collection by conducting interviews, reviewing medical charts, and accessing medical information systems.
• Assist with recruiting and screening subjects per IRB approved protocols.
• Assist in verifying participant eligibility; obtain consent and enrollment; ensure accurate demographic data for follow-up.
• Assist with data analysis and interpretation using descriptive statistics in SAS, STATA, and SPSS.
• Assist in developing, submitting, and providing content for grants, papers, abstracts, manuscripts, and presentations.
• Assist PI and team in developing research protocols and materials; provide study analysis and recommendations.
• Perform administrative duties and maintain communication with participants and colleagues regarding protocol information.
• Performs other duties as assigned.

Skills

Analytical thinking

Communication skills

Team collaboration

Independent judgment

Education

Bachelor's degree in a scientific field

Tools

SAS

STATA

SPSS

Job description

The University of Maryland, Baltimore (UMB) is seeking a detail-oriented researcher to support clinical studies in a professional setting. Responsibilities include recruiting subjects, collecting and organizing data, reviewing medical records, and ensuring protocol compliance.

The role requires independent judgment and collaboration with the research team to advance study objectives. Qualifications include a Bachelor’s degree in a scientific field and preferred clinical research experience.