Senior Research Scientist– Clinical Practice and Data Expert

Senior Research Scientist– Clinical Practice and Data Expert (Hybrid, Chicago Loop) Please include a CV, Cover Letter, and professional references upon request. Job Summary NORC at the University of Chicago is seeking an experienced Senior Research Scientist to lead and contribute to prescription drug programs and policy projects, with an emphasis on pharmaceutical drug prescribing practices and guidelines. This role can be full‑time or part‑time and requires a hybrid work schedule of at least two days a week in either our Chicago, IL or Washington, DC offices. Responsibilities Lead and contribute to growing NORC’s portfolio in clinical practice and prescription drug policy and research, specifically clinical and oncology pharmacy Conduct clinical practice guideline reviews and assess their impact on drug utilization Conduct FDA label reviews and synthesize clinical trial evidence Provide clinical consultation on prescribing practice requirements, and interpret comparative effectiveness based on clinical trial data Utilize data and literature to recognize domestic and global public health problems Develop protocols and conduct clinician/provider stakeholder interviews on pharmaceutical drug prescribing practices Develop protocols for and conduct clinical trial literature reviews and data extraction Conduct systematic reviews that appropriately summarize epidemiologic literature Provide input on contract proposals and grant applications related to clinical practice, pharmaceutical drug research, and analyses Communicate effectively with clients, consultants, and members of the policy and research community Participate in internal discussions and strategic thinking concerning future research opportunities Manage project deliverables closely with clients to ensure expectations are met with high quality and collegiality Manage project teams and provide pharmaceutical drug prescribing practice guideline expertise Mentor junior staff Required Skills Master’s in Pharmacy or Nursing; Doctoral degree in Pharmacy or Medicine preferred At least 9 years’ experience in clinical pharmacy or oncology pharmacy with responsibility for clinical practice guidelines and research‑based prescribing protocols Expert knowledge of pharmaceutical drug utilization, treatment recommendations, FDA labels, and clinical oncology pharmacy Ability to monitor and oversee administrative aspects of ongoing projects Expertise with analyzing pharmaceutical utilization and quality outcomes using data for payor programs (Medicare, Medicaid, commercial) Strong foundation in reviewing clinical trial research Managerial, leadership, and interpersonal skills to lead interdisciplinary, cross‑national project teams Excellent oral and written communication and coordination of multiple projects Occasional travel for site visits and meetings may be required Qualified applicants must be eligible to work in the U.S.; visa sponsorship not available Hybrid work schedule of at least two days a week in Chicago, IL or Washington, DC Salary and Benefits The pay range for this position is $133,000–$165,000. Benefits Generously subsidized health insurance, effective on the first day of employment Dental and vision insurance Defined contribution retirement program and voluntary 403(b) program Group life insurance, long‑term and short‑term disability insurance Work/life balance benefits: paid time off, holidays, paid parental leave, bereavement leave, tuition assistance, Employee Assistance Program (EAP) Equity, Diversity, and Inclusion We are an equal‑opportunity employer. We evaluate qualified applicants without regard to race, color, religion, sex, gender, national origin, disability, veteran status, sexual orientation, or other legally protected characteristics. #J-18808-Ljbffr