Director – Statistics

🔥 12 hours ago

🇺🇸 United States – Remote

💵 $166.5k - $338.8k / year

⏰ Full Time

🔴 Lead

👔 Director

👻 Ghost score 0%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Eli Lilly and Company

WebsiteLinkedInAll Job Openings

10,000+ employees

💊 Pharmaceuticals

🏥 Healthcare

🧬 Biotechnology

💰 $6.5M Post-IPO Debt - Eli Lilly on 2024-02

Pharmaceuticals • Healthcare • Biotechnology

Eli Lilly and Company is a global pharmaceutical company that researches, develops, manufactures, and distributes prescription medicines and provides patient support services. The company focuses on life-changing medicines across conditions such as diabetes, cancer, Alzheimer’s disease, autoimmune disorders, dermatology, migraine, obesity, and sleep apnea; it runs clinical trials, offers LillyDirect pharmacy services, and emphasizes manufacturing quality, medication safety, and research into genetic medicines. Eli Lilly also provides patient resources, condition education, and access programs to help people find care and participate in trials.

📋 Description

• Lead development of clinical plans, innovative study designs, statistical analysis, and interpretation of results at the program level • Shape the internal and external drug-development environment using analytical thinking and therapeutic-area knowledge • Enrich decision-making, identify efficiencies, and increase projects’ probability of technical success • Champion innovative statistical methodology and applications • Influence teams on critical risks and plan resolutions; integrate information and make data-driven decisions • Provide input on study protocols, design studies, and write study-conduct protocols • Select statistical methods, author protocol and statistical analysis plan sections, and conduct analyses after database creation • Collaborate with data sciences on data quality assurance plans • Maintain current knowledge and proficiency in statistical methodology and justify selected methods • Peer-review statistical colleagues’ work products • Influence team members regarding appropriate research methods • Collaborate on reports and communicate study results • Communicate results through regulatory submissions, manuscripts, oral presentations, customer discussions, and scientific meetings • Respond to regulatory queries and interact with regulators • Understand disease states, competitive landscapes, and regulatory environments • Perform work in compliance with applicable policies, procedures, processes, and training • Introduce and apply innovative methodology and tools to solve critical problems • Combine 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

🎯 Requirements

• Ph.D. in Statistics OR Biostatistics • At least 7 years of experience in clinical research and development in the Pharmaceutical Industry • Significant experience with clinical trials, medical research, and/or real-world evidence • An established track record of developing and maintaining an area of statistical or collaborative research • Proficient in statistical programming languages/software such as SAS, R, Spotfire, etc • Interpersonal communication skills for effective customer consultation and collaboration • Teamwork and leadership skills; ability to provide statistical leadership and technical expertise to influence business decisions • 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 • Business process expertise associated with critical activities (e.g., regulatory submissions) • Ability to follow applicable Corporate, Medical, local, and departmental policies, procedures, processes, and training

🏖️ Benefits

• Company bonus depending partly on company and individual performance • Company-sponsored 401(k) • Pension • Vacation benefits • Medical benefits • Dental benefits • Vision benefits • Prescription drug benefits • Healthcare and/or dependent day care flexible spending accounts • Life insurance and death benefits • Time off and leave of absence benefits • Employee assistance program • Fitness benefits • Employee clubs and activities • Disability accommodation support during the application process • Employee resource groups