Clinical Research Assistant B
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 BJob Profile Title
Clinical Research Assistant BJob Description Summary
The Clinical Research Assistant B will serve as the point of contact for all study related inquiries and will be responsible for coordinatingresearch related activities per protocol including recruitment, eligibility screening, running participant sessions, sample collection, data
collection and quality assurance.
Job Description
Job Responsibilities
- The successful candidate will have experience collecting research data, interacting with research participants and working well as part of a team.
- Specific activities include: (1) Serving as a point of contact for all study related inquiries; (2) Consenting participants; (3) Collecting behavioral
questionnaire data and biological samples; (4) Collect side effect data and follow reporting procedures; (5) Conducting data entry/quality
assurance; and (6) Performing additional duties as assigned.
Qualifications
- Qualified candidates should have a High School Grad/GE Degree and 3 to 5 years of experience or equivalent combination of education and experience is required. Experience
should include: previous experience recruiting and consenting research participants; previous experience working with clinical patient populations; familiarity with data collection and quality control procedures; and a demonstrated ability to prioritize and manage multiple projects while meeting deadlines. Preferred candidates will also demonstrate a customer service orientation, a high degree of professionalism, the ability to communicate effectively, a careful attention to detail, and an ability to commit to at least 12 months of service.
Position is contingent upon continued funding.
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