Senior Advisor - Statistics

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees work worldwide to discover and bring life‑changing medicines to those who need them, improve the understanding and management of disease, and give back to communities through philanthropy and volunteerism. We give our best effort to our work and put people first;

we’re looking for people determined to make life better for people around the world.

The Clinical Project Statistician develops or 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 Clinical Project Statistician is responsible for working with research associates and scientists to establish a reporting database and for analyzing data for clinical studies.

• Provide input on study protocol, design studies and write protocols for the conduct of each study.
• Be 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, maintain proficiency in applying new and varied methods, and be competent in justifying methods selected.
• 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, or oral presentations in group settings, as well as for communicating one‑on‑one with key customers and presenting at scientific meetings.
• Respond to regulatory queries and interact with regulators.

• Understand disease states, competitive landscapes, and regulatory environment in order to enhance the level of customer focus and collaboration and be seen as a strong scientific contributor.

• Perform work in full compliance with assigned curriculum(s) and will be responsible for following 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 OR Biostatistics with at least 3 years of experience in Clinical Research and Development.

• Proficient in statistical programming languages/software such as SAS, R, Spotfire, WinBUGs, etc.
• 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.

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form () for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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