Clinical Research Coordinator

Location: Northern

## Clinical Research Coordinator Apply:
Hybrid Eligible:
3535 Market:
Full time:
Posted Today:
JR
** 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
** Job Profile Title
** Clinical Research Coordinator B
** Job Description Summary
** Clinical Research Coordinator B will conduct in-home and on-site study visits; will distribute participant incentives to participants; will conduct literature reviews and synthesis; assist in coding of interviews; prepare and process all Institutional Review Board (IRB) through the IRB and other regulatory groups as appropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events; coordinate, organize and maintain all documentation required by sponsor or CRO (case report forms, source documentation, study and regulatory binders, subject binders), Adhere to all University of Pennsylvania, ICF, and FDA guidelines and NIH policies, preparation of manuscripts and findings for presentation, and will provide administrative support for research operations;

participate in weekly study progress meetings with the PI and research team.
** Job Description
** Clinical Research Coordinator B will conduct in-home and on-site study visits; will distribute participant incentives to participants; will conduct literature reviews and synthesis; assist in coding of interviews; prepare and process all Institutional Review Board (IRB) through the IRB and other regulatory groups as appropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events; coordinate, organize and maintain all documentation required by sponsor or CRO (case report forms, source documentation, study and regulatory binders, subject binders), Adhere to all University of Pennsylvania, ICF, and FDA guidelines and NIH policies, preparation of manuscripts and findings for presentation, and will provide administrative support for research operations;

participate in weekly study progress meetings with the PI and research team.  CRC B will manage IRB submissions and renewals in accordance with FDA and IRB guidelines, assure compliance with the protocol and regulatory requirements including collecting, recording, and maintaining data and source documentations. Promote good clinical practice in the conduct of clinical investigations, including possessing an in-depth knowledge of the federal regulations and guidance documents for the conduct of clinical studies and human subject protection.  

Position is contingent on funding  
** Job Responsibilities**
* ** Talking to participants to determine interest in participating in research**
* ** Verbally walking participants through consent procedures**
* ** Administering study protocol**
* ** Overseeing data entry in study data set**
* ** Distributing study recruitment materials**
* ** Traveling between study visits**
* ** Perform additional duties as assigned*
* ** Qualifications
* ** Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required.
** Job Location - City, State
** Philadelphia,…