Associate Director, Epidemiological Statistical Programming

Job not on LinkedIn

🕒 August 18

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

⏰ Full Time

🟠 Senior

👔 Director

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 25%

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.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Clinical Outcomes Solutions

WebsiteLinkedInAll Job Openings

51 - 200 employees

💼 Consulting

🏥 Healthcare

🧬 Biotechnology

Consulting • Healthcare • Biotechnology

Clinical Outcomes Solutions is a global clinical outcomes consultancy that provides comprehensive support and services in all aspects of Clinical Outcome Assessment (COA) research. The company helps inform patient care by capturing the patient voice through innovative scientific methods. It guides organizations in navigating the complexities of clinical outcomes research by crafting strategies and solutions to capture accurate data. Trusted by pharmaceutical and biotechnology companies, the firm ensures regulatory compliance and optimized patient outcomes.

📋 Description

• Provide technical and functional leadership to statistical programmers supporting epidemiological and real-world evidence studies • Lead and contribute hands-on to statistical programming activities across multiple therapeutic areas • Develop, validate, and maintain SAS and/or R programs for analysis datasets, statistical outputs, tables, figures, and other data products • Partner with epidemiologists, statisticians, data scientists, and cross-functional stakeholders on programming approaches • Provide expert technical consultation on complex programming, data, and analytical challenges • Oversee and review programming deliverables for accuracy, reproducibility, quality, timelines, and standards • Support programming using administrative claims, electronic health records, registries, and other healthcare databases • Develop analysis-ready datasets, programming specifications, derivation logic, quality-control procedures, and documentation • Establish programming standards, reusable tools, macros, code libraries, documentation, and quality-control processes • Drive automation, standardization, continuous improvement, and scalable programming approaches • Plan and prioritize programming activities, identifying resource needs, risks, dependencies, and delivery challenges • Support regulatory and health authority requests, publications, abstracts, presentations, and evidence-generation activities • Ensure compliance with regulatory requirements, company policies, SOPs, data privacy requirements, and industry best practices • Develop and maintain SOPs, work instructions, programming conventions, and related documentation • Foster collaboration and develop programming talent through coaching, knowledge sharing, technical review, and mentorship

🎯 Requirements

• Bachelor’s degree or higher in Statistics, Biostatistics, Epidemiology, Computer Science, Data Science, Mathematics, or a related quantitative discipline • 8+ years of relevant statistical programming experience in pharmaceutical, biotechnology, CRO, healthcare, or life sciences industry • Demonstrated experience supporting epidemiological, observational, real-world evidence (RWE), HEOR, and/or related research • Experience with Optum and Truveta • Advanced programming expertise in SAS and/or R • Ability to develop, validate, and maintain complex analytical programs and reproducible programming workflows • Strong experience with large and complex healthcare data sources, including administrative claims, EHRs, patient registries, or other real-world data • Understanding of epidemiological study designs, statistical analysis methods, and programming techniques for observational and real-world research • Ability to provide technical leadership and guidance, mentor colleagues, review programming approaches and deliverables, and resolve complex technical challenges • Experience leading or coordinating programming activities across multiple projects • Experience overseeing and reviewing programming deliverables • Experience with line managing a team • Commitment to programming quality, reproducibility, documentation, standards, and best practices • Ability to work independently, exercise sound technical judgment, and manage multiple priorities • Excellent written and verbal communication skills • Strong collaboration and leadership skills across multidisciplinary and geographically dispersed teams

🏖️ Benefits

• Consistent training, development, and support • Significant professional growth for employees