Sr. Advisor - Statistics; RWE

Overview

The Clinical Project Statistician develops and assists in the development of protocol designs, clinical plans, and data analysis plans in collaboration with physicians, clinical research scientists, and other research colleagues. The role involves working with research associates and scientists to establish a reporting database and analyze data for clinical studies.

• Provide input on study protocol, design studies, and write protocols for each study.
• Accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the protocol and the statistical analysis plan, and conducting the actual analysis once a reporting database is created.
• Collaborate with data sciences in the planning and implementation of data quality assurance plans.
• Maintain currency with respect to statistical methodology, stay proficient in applying new and varied methods, and justify selected methods.
• Perform peer‑review of work products from other statistical colleagues.
• Influence team members regarding appropriate research methods.
• Collaborate with team members to write reports and communicate results.
• Assist with, or be responsible for, communicating study results via regulatory submissions, manuscripts, oral presentations, and presentations at scientific meetings.
• Respond to regulatory queries and interact with regulators.
• Understand disease states, competitive landscapes, and regulatory environment to enhance customer focus and collaboration as a strong scientific contributor.
• Perform work in full compliance with assigned curriculum(s) and follow applicable corporate, medical, local, and departmental policies, procedures, processes, and training.
• Introduce and apply innovative methodology and tools to solve critical problems.
• Merge scientific thinking and business knowledge to identify issues, evaluate options, and implement solutions.
• Lead projects independently and work effectively across functions.
• Apply technical expertise to influence business decisions.

• Ph.D. in Statistics, Biostatistics, Epidemiology, or Computer Science.
• At least 3 years of experience in Real World Evidence research.

• Proficiency in statistical programming languages/software such as SAS, R, Spotfire, WinBUGs.
• Strong interpersonal communication skills for effective customer consultation.
• Teamwork and leadership skills.
• Technical expertise and application with working knowledge of experimental design and statistical analysis.
• Self‑management skills with a focus on results for timely and accurate completion of competing deliverables.
• Resource management skills.
• Creativity and innovation.
• Demonstrated problem‑solving ability and critical thinking.

• Anticipated wage range: $151,500 – $244,200.
• Full‑time employees eligible for company bonus (depending on company and individual performance).
• Comprehensive benefit program including 401(k) participation, pension, vacation benefits, medical, dental, vision, prescription drug benefits, flexible spending accounts, life and death insurance, leave of absence benefits, employee assistance program, fitness benefits, and employee clubs.
• Benefits are subject to amendment, modification, or termination at Lilly’s discretion.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

If you require accommodation to submit a resume for this position, please complete the accommodation request form at  Please note this request is for individuals to request an accommodation as part of the application process; any other correspondence will not receive a response.