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Part-Time Clinical Research Assistant B

University of Pennsylvania Perelman School of Medicine
Biomedical Research Building 2, United States, United Statespart_timeVerifiedPosted 10 Feb 2026
💰 $44,000/yr

About the role

University Overview

The University of Pennsylvania, the largest private employer in Philadelphia, is a world-renowned leader in education, research, and innovation. This historic, Ivy League school consistently ranks among the top 10 universities in the annual U.S. News & World Report survey. Penn has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn’s distinctive interdisciplinary approach to scholarship and learning. As an employer Penn has been ranked nationally on many occasions with the most recent award from Forbes who named Penn one of America’s Best Large Employers in 2023.

Penn offers a unique working environment within the city of Philadelphia. The University is situated on a beautiful urban campus, with easy access to a range of educational, cultural, and recreational activities. With its historical significance and landmarks, lively cultural offerings, and wide variety of atmospheres, Philadelphia is the perfect place to call home for work and play.

Posted Job Title

Part-Time Clinical Research Assistant B

Job Profile Title

Clinical Research Assistant B

Job Description Summary

This position is part of the Carroll laboratory. The laboratory works to better understand the biology of acute myeloid leukemia (AML) and to develop novel therapeutics. Primary responsibility will be assistance with development of AML patient registries. The laboratory works to understand the biology of AML in different ethnic groups. Individual will work with the tissue bank registry and further collect and annotate clinical information on patients with leukemia. Additional projects will provide annotation on clinical details and therapy outcomes to correlate with molecular studies in the laboratory or with collaborators. Will interact with clinical trial teams and will be trained in appropriate handling of confidential patient information.

Job Description

Job Responsibilities

  • Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols
  • Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
  • Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses
  • Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports. See more occupations related to this task.
  • Inform patients or caregivers about study aspects and outcomes to be expected.
  • Collect data (physiological, paper and pencil measures, dietary recalls, and computerized laboratory tasks) per study protocol. Complete data entry and quality assurance assignments. (45% Essential: 1),Conduct scripted telephone eligibility screenings (30% Essential: 1),Act as primary point of contact for study participants; schedule appointments; conduct reminder calls; oversee in-person session prep (10% Essential: 1),Collect, process, log and ship samples (e.g., urine and saliva) according to study-specific protocols and maintain the cleanliness of lab spaces (5% Essential: 1),Report the progress of study participants per established SOPs. Maintain participant charts. Attend study meetings as required. (5% Essential: 1),Other duties and responsibilities as assigned. (5% Essential: 0)
  • Other duties and responsibilities as assigned

Position is contingent upon funding.

Qualifications

  • High School Grad/GE Degree and 3 to 5 years of experience or equivalent combination of education and experience is required.

Job Location - City, State

Philadelphia, Pennsylvania

Department / School

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