Clinical Research Assistant B (Division of Addictions)
University of PennsylvaniaAbout 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.
The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.
Posted Job Title
Clinical Research Assistant B (Division of Addictions)Job Profile Title
Clinical Research Assistant BJob Description Summary
Research Assistant will: (1) place recruitment advertisements, screen participants for eligibility, and schedule participants; (2) administer self-report measures at baseline and conduct baseline smoking rate assessments;(3) conduct two in-person laboratory assessments of reward and reinforcement; (4) conduct six weekly lab visits to assess CO, e-cigarette and cigarette use across 6 weeks; and (5) follow up with participants who reschedule or fail to show for an appointment, enter the study data, and ensure adequate study-related supplies.
Job Description
Job Responsibilities
Conduct participant eligibility screens. Review ICF and HIPAA forms with potential participants, answer questions, obtain signatures and maintain regulatory consent binders. Conduct participant laboratory sessions and data entry. This includes
administering questionnaires and computer tasks, collecting physiological data, collecting and processing samples, collecting and reporting side effects, and entering data. Maintain participant charts; conduct regular milestone and chart QA. Prepare documents (e.g. pulling charts, logs, etc.) necessary for monitoring visits. Perform additional duties as assigned.
* Conduct participant recruitment, completing in-clinic eligibility screens.
* Review Consent and HIPAA forms with potential participants, answer any ques tions, obtain signatures and maintain regulatory consent binders.
* Collect behavioral questionnaire data. Conduct data entry/QC and pre-processing of data as necessary.
* Conduct participant laboratory sessions and data entry as needed. This includes administering questionnaires and computer tasks, collecting physiological data, collecting and processing samples, collecting and reporting side effects, and scanning and manually entering data.
* Maintain participan
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