Uchicago
Clinical Research Project Manager
Chicago, IL · Part-time
Sponsorship not specified$75k-$90kDetected 7 hours ago
Data AnalysisStatisticsComplianceProject ManagementExcelHIPAAClinical TrialsClinical ResearchPublic HealthFDA RegulatorySTATAScientific WritingResearchLeadershipCommunicationProblem SolvingCritical ThinkingPublic SpeakingMicrosoft OfficeEpidemiology
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15Unrated
Cap-exempt (no lottery)0
Sponsors this role0
Entry-level history0
PERM / green-card track0
Lottery odds (Level I)39
Fits your clock70
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About the role
- Provides input into the strategic, administrative, operational, and financial decisions that impact clinical research conducted across the University.
- The job includes management of and research participation in the Bionic Breast project and other research studies involving human subjects.
- Ensures compliance of research activities with institutional, state, and federal regulatory policies, procedures, directives, and mandates.
Responsibilities
- Perform significant role in the design, development and implementation of quantitative and qualitative research studies, including grant writing, survey development, participant recruitment/enrollment/interviewing.
- Recognize abnormal results and varying conditions or procedures to correct problems, set up and perform experiments. Analyze meaning, significance, causes, and effects of the subject.
- Support compliant conduct, regulatory, and administrative activities. Stay current with and manage regulatory processes including IRB, FDA, NIH, HIPAA, CITI, clinicaltrials.gov, Florence portal.
- Support compliant conduct, regulatory, and administrative activities.
- Prepare and lead presentations and manuscripts, including as first author and presenter, for the purposes of presentation at scientific meetings and publication in peer-reviewed literature.
- Support compliant conduct, regulatory and administrative activities, including leading development and management of IRB protocols, by liaising with peer experts in these domains.
- Independently tracks data collection progress, identifies deviations from projected accrual plans, directs solutions to correct course, collaborates with research operations lead to ensure data collection progresses on budget and on time.
- Performs and supervises others in literature search, synthesis and citation management, ensuring best practices.
- Performs various professional, organizational, and operational tasks under limited supervision.
- Performs other related work as needed.
Requirements
- include a college or university degree in related field.
- Strong analytic skills as well as proficiency in STATA, R or equivalent programs required
- Proven expert level proficiency in Microsoft Word, Excel, PowerPoint, and scientific search engines.
- Uses in-depth knowledge of clinical studies to coordinate the collection of analyzable clinical research data and/or samples with a high degree of independence.
Nice to have
- Preferred Competencies
Skills
- Excellent critical thinking/problem solving skills.
- Demonstrated leadership, interpersonal and relationship building skills.
Compensation
- $75,000.00 - $90,000.00 The included pay rate or range represents the University's good faith estimate of the possible compensation offer for this role at the time of posting.
- The University of Chicago's Annual Security & Fire Safety Report (Report) provides information about University offices and programs that provide safety support, crime and fire statistics, emergency response and communications plans, and other policies and information.
Benefits
- Yes The University of Chicago offers a wide range of benefits programs and resources for eligible employees, including health, retirement, and paid time off.
- Information about the benefit offerings can be found in the Benefits Guidebook.
Equal opportunity
- Job seekers in need of a reasonable accommodation to complete the application process should call 773-702-5800 or submit a request via Applicant Inquiry Form.
- Job seekers in need of a reasonable accommodation to complete the
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