Clinical Research Coordinator A/B (Department of Neuroscience of Depression/Stress)
University of Pennsylvania Perelman School of MedicineAbout 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 Coordinator A/B (Department of Neuroscience of Depression/Stress)Job Profile Title
Clinical Research Coordinator AJob Description Summary
The Center for Neuromodulation in Depression and Stress at the University of Pennsylvania is looking for a Clinical Research Coordinator, A or Clinical Research Coordinator B to join our team. The research coordinator will work full-time on a variety of research studies focused on the neuroscience of depression. The position is contingent on continued funding.CRC A: The research coordinator A will work closely with the principal investigator as well as other collaborating investigators and CNDS staff in carrying out CNDS research. S/he will be trained to conduct human neuroimaging research with a number of tools, including transcranial magnetic simulation (TMS), magnetic resonance imaging (MRI), and psychophysiology tools such as electromyography and electrocardiography. S/he will also be trained to administer clinical scales with psychiatric patients. Primary responsibilities include collecting, maintaining, and organizing all questionnaires, assessments, demographic data, and imaging data of the participants. Additionally the coordinator will conduct recruitment, will screen and enroll potential study patients as specified per protocol, and the coordinator will also perform regulatory duties such as preparation and submission of regulatory documents through the IRB (initial submissions, amendments, and continuations). The research coordinator should be interested in and capable of developing skills across a number of research methodologies, neuroimaging software, and data analysis tools. Work hours will include evenings and Saturdays as needed to accommodate MRI scan calendar openings. The coordinator will also be trained to administer Transcranial Magnetic Stimulation (TMS).
CRC B: The research coordinator B will work full-time on a variety of research studies focused on the neuroscience of depression. Primary duties include preparing protocols, informed consents, and advertisements. Additionally this position will coordinate study recruitment, screening study participants for inclusion in CNDS studies, scheduling and running study visits, administration of cognitive and psychological assessments, and accompanying participants to the neuroimaging scanners and running neuroimaging protocols. The research coordinator will work closely with the principal investigator and the data analysts in the implementation of study databases. The coordinator is also responsible for data collection and data management in accordance with study protocol and the maintenance of individual patient data, source documents, case report forms, and regulatory duties: prepare and submit regulatory documents through the IRB (initial submissions, amendments, continuations). The coordinator will also be trained to administer Transcranial Magnetic Stimulation (TMS).
The research coordinator will be responsible for reviewing and entering the data into the study database and assisting with data analysis. He/she will also help with submitting recruitment reports to the NIH and will maintain th
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