NORC at the University of Chicago
Senior Research Scientist– Clinical Practice and Data Expert - Hybrid Chicago Lo
NORC at the University of Chicago, Chicago, Illinois, United States, 60290
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.
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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