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Regulatory Affaires Specialist / Senior Regulatory Affairs Specialist
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 Employers By State in 2021.
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.
COVID-19 vaccination is a requirement for all positions at the University of Pennsylvania. New hires are expected to be fully vaccinated before beginning work at the University. For more information about Penn's vaccine requirements and the use of Penn Open Pass, visit the Penn COVID-19 Response website for the latest information.
Posted Job Title
Regulatory Affaires Specialist / Senior Regulatory Affairs Specialist
Job Profile Title
Regulatory Affairs Specialist
Job Description Summary
The newly established Immune Health Initiative is hiring a full-time Regulatory Affairs Specialist or Senior Regulatory Affairs Specialist to assist with departmental IRB maintenance and submissions and to perform routine internal study monitoring for all observational clinical research studies. Research in this group is focused on understanding human immune health across multiple study cohorts spanning adult to pediatric medicine patients as well as healthy subjects.
Position contingent upon funding.
Job Description
The position will write and manage regulatory documents that will promote human subjects research and clinical trials for investigator-initiated studies at the University of Pennsylvania. This position will provide expertise and support to investigators seeking to initiate with human subjects' research and will facilitate communication with the research team, organize the submission process, write and edit study documentation, and provide regulatory expertise. The Regulatory Specialist will read and understand proposal requirements and develop a plan for proposal completion including collecting proposal components, determining timelines, and maintaining a collaborative workplace. They will be responsible for all regulatory aspects of Institutional Review Board (IRB) documentation including continuing reviews, amendments, and reporting of adverse events and deviations. The regulatory specialist will monitor IRB compliance and take corrective steps when needed. They will ensure all documents and files are organized and maintained in accordance with protocols. The successful candidate is expected to resolve regulatory and data queries in a timely manner. Additionally, the Regulatory Specialist will maintain regulatory documents and information by building and maintaining REDcap databases as needed.
In addition to the above, the Regulatory Affairs Specialist Senior position will manage activities of and train junior regulatory specialists as well as train CRCs in the larger clinical group and take a leadership role in making sure all regulatory and compliance needs are met across multiple protocols. Develop SOP as needed.
Qualifications:
For regulatory specialist, a Bachelor's Degree and 3-5 years of direct regulatory experience or equivalent combination of education and experience required. For senior regulatory specialist 5-7 yrs experience or equivalent combination of education and experience required. This position requires excellent oral and written communication skills to interact with clinicians, clinical research coordinators and program director. Prior experience with IRB guidelines and submissions, IRB protocol compliance and policies, human subject research practices and professional skills in the execution of clinical research protocols is required. REDcap experience is required as well as strong computer skills with proficiency in accessing, sharing, and modifying documents (excel, work, google docs, etc) across platforms. Excellent organization, attention to detail and strong problem-solving skills are required. Must be able to work in a team environment.
This position is contingent upon grant funding.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$51,824.00 - $78,096.00
Affirmative Action Statement
Penn adheres to a policy that prohibits discrimination on the basis of race, color, sex, sexual orientation, gender identity, religion, creed, national or ethnic origin, citizenship status, age, disability, veteran status, or any other legally protected class.
Special Requirements
Background check required after a conditional job offer is made. Consideration of the background check will be tailored to the requirements of the job.
University Benefits
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