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The University of Pennsylvania in Philadelphia, PA, seeks a Clinical Research Project Manager C to oversee regulatory affairs and multi-study coordination within the Department of Medicine Clinical Trials Unit (DOM CTU). You will manage regulatory submissions, quality controls, and staff development across diverse clinical trials.
Requires a Master’s degree and 5–7 years of clinical research experience, with strong knowledge of IRB processes and GCP.
The University of Pennsylvania, the largest private employer inPhiladelphia, is a world-renowned leader in education, research,and innovation. This historic, Ivy League school consistently ranksamong the top 10 universities in the annual U.S. News & WorldReport survey. Penn has 12 highly-regarded schools that provideopportunities for undergraduate, graduate and continuing education,all influenced by Penn's distinctive interdisciplinary approach toscholarship and learning. As an employer Penn has been rankednationally on many occasions with the most recent award from Forbeswho named Penn one of America's Best Large Employers in 2023.
Penn offers a unique working environment within the city ofPhiladelphia. The University is situated on a beautiful urbancampus, with easy access to a range of educational, cultural,andrecreational activities. With its historical significance andlandmarks, lively cultural offerings, and wide variety ofatmospheres, Philadelphia is the perfect place to call home forwork and play.
The University offers a competitive benefits package that includesexcellent healthcare and tuition benefits for employees and theirfamilies, generous retirement benefits, a wide variety ofprofessional development opportunities, supportive work and familybenefits, a wealth of health and wellness programs and resources,and much more.
Clinical Research Project Manager C
Clinical Research Project Manager C
The Department of Medicine Clinical Trials Unit (DOM CTU) supportsa diverse group of investigators, involving work on a wide spectrumof clinical trials ranging from phase I to IV, investigator andindustry initiated, different disease states and varyingcomplexities. Our projects occur throughout the Department ofMedicine including Cardiology, Pulmonary, Rheumatology,Translational Medicine, Gastroenterology, Infectious Disease,General Medicine, Sleep, HemOnc, Endocrine, Renal and Geriatrics.To learn more about DOM CTU visit https://www.med.upenn.edu/pennctu/.
The Regulatory/Project Manager C provides regulatory expertise andoversight, project management, and staff supervision for theDepartment of Medicine Clinical Trials Unit (DOM CTU). The positionsupports studies across disease areas, phases, and levels ofcomplexity, combining hands-on work with senior-level consultation,regulatory planning, and leadership of complex projects whenassigned. The manager independently performs and overseesregulatory activities, manages studies from intake throughclose-out, supervises and develops staff, and improves studyquality and operational effectiveness. Additional responsibilitiesinclude securing funded work for this position, pursuing work forother DOM CTU staff to support unit-wide sustainability, andcoordinating routine unit administration.
The Regulatory/Project Manager C provides regulatory expertise andoversight, project management, and staff supervision for theDepartment of Medicine Clinical Trials Unit (DOM CTU). The positionsupports phase I-IV, investigator-initiated, and industry-sponsoredresearch across disease areas and levels of complexity.Responsibilities combine hands-on support and ongoing studymanagement with senior-level consultation and leadership of complexprojects when assigned.
The position independently prepares and oversees regulatorysubmissions, documentation, and approvals; serves as a seniorregulatory resource; advises on regulatory approaches; and resolvescomplex compliance issues. Responsibilities includeaudit/inspection preparation and responses, corrective actions,regulatory SOPs and quality-review processes, and IND/IDE exemptionassessments and submissions when included in assignedservices.
The manager leads study intake, feasibility, start-up,implementation, and close-out; develops project plans and studytools; and contributes to protocol and grant development, budgets,and resource planning. The position leads project teams, resolvesoperational barriers, develops performance metrics, and monitorsstudy quality, recruitment, scope, budgets, and deliverables. Themanager advises on resource deployment and implements improvementsacross assigned projects.
The position directly supervises assigned research staff, includingwork assignment, workload and quality monitoring, onboarding,training, coaching, and performance evaluation. The managerparticipates in recruitment, addresses performance and developmentneeds, and promotes consistent use of SOPs, study tools, and bestpractices across assigned teams.
Additional responsibilities include proactively marketing DOM CTUstaff and services, taking primary responsibility for securingfunded work to sustain this position, and sharing responsibilityfor pursuing and securing assignments for other CTU staff tosupport unit-wide financial sustainability. The manager alsocoordinates routine unit administration, performing or delegatingtasks while remaining accountable for timely completion.
Master's degree and 5-7 years of related clinical researchexperience, or an equivalent combination of education andexperience required. Progressively responsible experience inregulatory affairs, clinical research project management, and staffsupervision. Demonstrated ability to independently manage assignedstudies and regulatory work, coordinate multiple stakeholders, andsupervise, train, and evaluate staff.
Demonstrated knowledge of IRB processes, human research protectionrequirements, Good Clinical Practice, and regulatory documentation.Strong written and verbal communication, planning, organization,problem solving, attention to detail, and follow-through. Abilityto manage competing priorities, anticipate and resolvestudy-related problems, maintain study quality, and meet deadlines.Proficiency with standard office, collaboration,andresearch-tracking tools.
Experience in academic clinical research, SOP development, stafftraining, process improvement, and electronic regulatory documentsystems. A relevant master's degree or research/regulatorycertification is preferred. IND/IDE submission experience whenrelevant to assigned services, and experience communicatingresearch services and developing collaborations, arepreferred.
Philadelphia, Pennsylvania
Perelman School of Medicine
$91,066.00 - $106,940.00 Annual Rate
Salary offers are made based on the candidate's qualifications,experience, skills, and education as they directly relate to therequirements of the position, and in alignment with salary rangesbased on external market data for the job's level. Internalorganization and peer data at Penn are also considered.
The University of Pennsylvania is an equal opportunity employer.Candidates are considered for employment without regard to race,color, sex, sexual orientation, religion, creed, national origin(including shared ancestry or ethnic characteristics), citizenshipstatus, age, disability, veteran status or any class protectedunder applicable federal, state or local law.
Background checks may be required after a conditional job offer ismade. Consideration of the background check will be tailored to therequirements of the job.
To learn more, please visit: https://www.hr.upenn.edu/PennHR/benefits-pay
Equal Employment Opportunity Statement
The University of Pennsylvania is an equal opportunity employer.Candidates are considered for employment without regard to race,color, sex, sexual orientation, religion, creed, national origin(including shared ancestry or ethnic characteristics), citizenshipstatus, age, disability, veteran status or any class protectedunder applicable federal, state, or local law.