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Yi Peng Email & Phone Number

Director, RWE Analytics, Value and Evidence at AbbVie
Location: Greater Minneapolis-St. Paul Area, United States 11 work roles 2 schools
1 work email found @abbott.com LinkedIn matched
✓ Verified August 2026 4 data sources Profile completeness 100%

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Current company
Role
Director, RWE Analytics, Value and Evidence
Location
Greater Minneapolis-St. Paul Area, United States
Company size

Who is Yi Peng? Overview

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Yi Peng is listed as Director, RWE Analytics, Value and Evidence at AbbVie, a with 57013 employees, based in Greater Minneapolis-St. Paul Area, United States. AeroLeads shows a work email signal at abbott.com and a matched LinkedIn profile for Yi Peng.

Yi Peng previously worked as Director, RWE Analytics, Value & Evidence at Abbvie and Associate Director, RWE Analytics, Value & Evidence at Abbvie. Yi Peng holds M.S., Biostatistics from University Of Minnesota.

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{first}.{last}@abbott.com
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Profile bio

About Yi Peng

1. Collaborated with cross-functional teams, including HEOR TA scientists, Medical Affairs, Commercial, and KOLs, in a matrix working environment in the pharmaceutical industry.2. Utilized Real World Data (RWD), including large administrative claims database (Medicare/Optum/MarketScan), electric health records (Optum Market Clarity/IBM Watson/EPIC/Japan MDV), registry data (USRDS/SRTR), and national survey data (NHANES/NHIS/MCBS), to develop study concepts, design studies, conduct statistical modeling/programming, and disseminate results in various areas, such as epidemiology, health economics, policy, and outcome research.3. Conducted projects on studying healthcare resource utilization/cost, comparativeness effectiveness, treatment patterns, medication adherence/interruption, burden of illness, and incidence/prevalence using RWD in therapeutic areas, including oncology, hematology, nephrology, cardiology, rheumatology, transplantations, bone mineral diseases, etc.4. Designed and conducted Patient Report Outcomes analyses using clinical trials data.5. Conducted indirect treatment comparisons (like MAIC and Bayesian NMA) by utilizing patient-level and aggregate-level clinical trial data to compare effectiveness and safety endpoints.6. Co-authored over 30 peer-reviewed journal publications and presented over 100 conference abstracts.7. Managed a team of project managers, statisticians, and programmers for more than 8 years.8. Possesses excellent organizational, interpersonal, presentation, communication, and writing skills.9. Google scholar link: https://scholar.google.com/citations?user=NU0H_1oAAAAJ&hl=en

Listed skills include Sas, Biostatistics, Statistics, Survival Analysis, and 33 others.

Current workplace

Yi Peng's current company

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AbbVie
Abbvie
Director, RWE Analytics, Value and Evidence
Saint Paul, MN, US
Website
Employees
57013
AeroLeads page
11 roles

Yi Peng work experience

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Director, Rwe Analytics, Value And Evidence

Saint Paul, Mn, Us

Director, Rwe Analytics, Value & Evidence

Current

North Chicago, Illinois, Us

Nov 2024 - Present

Associate Director, Rwe Analytics, Value & Evidence

North Chicago, Illinois, Us

• Collaborate with HEOR TA scientists and other stakeholders to translate HEOR business needs into research concepts using real-world evidence (RWE), and participate in planning, designing, executing, and disseminating results of RWE studies.• Utilize real-world data to conduct observational studies aimed at assessing unmet patient needs, disease burden, treatment effectiveness, and adverse events.• Perform indirect treatment comparisons (such as MAIC and Bayesian NMA) using patient-level and aggregate-level clinical trial data to compare efficacy and safety endpoints.• Manage analytical activities for multiple studies, focusing on RWE analyses from large observational databases (e.g., medical claims, EMR/EHR, registries), as well as conducting Patient Reported Outcomes analyses in clinical trials data across the rheumatology and pan-immunology therapeutic areas.• Foster effective cross-functional relationships to ensure teamwork and problem-solving within the analytics team and with CRO.• Ensure the completion of all projects with high quality and within the specified timeline, despite the complexities of a matrix organizational structure.

Jan 2022 - Nov 2024

Director Of Analytics

Minneapolis, Minnesota, Us

• Worked closely with clients from biotech and pharmaceutical companies to identify real world evidence (RWE) needs in products development, pre- and post-approval regulatory requirements, and benefit & risks assessment. Develop study concept, design, and execute observational studies using various epidemiological designs and statistical methods in Real World Data (RWD). Collaborate with biopharma clients to disseminate study results in report, conference abstracts and peer-reviewed publications.• Worked with government agencies and principal investigators and lead the effort in supporting the United State Renal Data System (USRDS), a NIH funded government contract. I work with a cross functional team (Physician Investigators, epidemiologists, IT, project manager, statisticians, and programmers) to ensure deliverables in high quality and meeting timelines. My team constructs and maintains the entire data system, conducts analyses, and generates results for USRDS annual/quarterly report, online data visualization tools (R-Shiny application), and publications. • Oversaw a team of project managers, statisticians and programmers on study planning, budgeting, study protocol and statistical analysis plan (SAP) development, statistical analyses and results dissemination.• Developed standard operation procedures to streamline projects implementation and analytical process to improve efficiency.

Apr 2013 - Jan 2022

Clinical Statistician

Eagan, Mn, Us

• Collaborated with Pharmacists and physicians to identify the most appropriate study design to PBM business needs, performed statistical analyses, interpreted findings to non-statistical audiences, documented and published findings.• Created analytical datasets from large commercial insurance claims data warehouse to find members using complex date logic, ICD-9 diagnosis, and procedure code algorithms, and transformed files containing medical and pharmacy costs for statistical analyses.• Analyzed and reported cost or event avoidance impact of clinical programs such as medical policies, utilization management policies, and drug adherence. Analyzed health care claims data (medical and pharmacy claims) using biostatistical, pharmacoeconomic techniques such as propensity score matching, generalized linear models and difference-in-difference approach.Abstract: Gleason PP, Peng Y, Starner CI. Immunosuppressant Waste Associated with 90-Day Supplies Compared with 30-Day Supplies of Calcineurin Inhibitors. Academy of Managed Care Pharmacy: San Diego, CA, April 2013. Published: J Manag Care Pharm 2013;19(2):170-171.

Jun 2012 - Mar 2013

Biostatistician Iii

Minneapolis, Minnesota, Us

• Participated in epidemiological study design, performed statistical analyses, and prepared study report to support pharmaceutical companies sponsored observational research studies and government funded contracts. The work were generally epidemiological studies which evaluated trends in diseases incidence/prevalence, burden of illness, adverse events/outcomes, and therapies for patients. • Worked with operational researchers, liver surgeons in developing Liver Simulated Allocation Models (LSAM) to support liver allocation policy development in the U.S.• Lead Biostatistician in designing and analyzing pre- and post-liver transplant outcome studies using national solid organ transplantation database (OPTN/SRTR). • Participated in conference abstracts and peer-reviewed journal publications submission and provided statistical support.

Jan 2012 - Jun 2012

Research Assistant

Minneapolis And St. Paul, Minnesota, Us

Assisted Dr. Lynn Eberly to perform statistical analysis for a grant application using MRFIT (the Multiple Risk Factor Intervention Trial) data. Analytical methods included Logistic Regression, Survival Analysis, Longitudinal analysis.

Aug 2005 - May 2006

Technical Support Engineer

Shenzhen, Guangdong, Cn

Maintained telecommunication equipments and large relational databases (Oracle, SQL server). Provided remote and on-site technical services to our customers on telecommunication systems. Provided technical training for customers and subcontractors.

Aug 2001 - Aug 2003
Team & coworkers

Colleagues at AbbVie

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2 education records

Yi Peng education

M.S., Biostatistics

University Of Minnesota

B.S., Mathematics

Dalian University Of Technology
FAQ

Frequently asked questions about Yi Peng

Quick answers generated from the profile data available on this page.

What company does Yi Peng work for?

Yi Peng works for AbbVie.

What is Yi Peng's role at AbbVie?

Yi Peng is listed as Director, RWE Analytics, Value and Evidence at AbbVie.

What is Yi Peng's email address?

AeroLeads has found 1 work email signal at @abbott.com for Yi Peng at AbbVie.

Where is Yi Peng based?

Yi Peng is based in Greater Minneapolis-St. Paul Area, United States while working with AbbVie.

What companies has Yi Peng worked for?

Yi Peng has worked for Abbvie, Hennepin Healthcare Research Institute, Prime Therapeutics, University Of Minnesota, and Huawei.

Who are Yi Peng's colleagues at AbbVie?

Yi Peng's colleagues at AbbVie include Donald Halbert, Vivian Prindle, Müge Rodop, Muzammal Khan, and Daniel Dima.

How can I contact Yi Peng?

You can use AeroLeads to view verified contact signals for Yi Peng at AbbVie, including work email, phone, and LinkedIn data when available.

What schools did Yi Peng attend?

Yi Peng holds M.S., Biostatistics from University Of Minnesota.

What skills is Yi Peng known for?

Yi Peng is listed with skills including Sas, Biostatistics, Statistics, Survival Analysis, R, Statistical Modeling, Sas Programming, and Clinical Research.

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