Senior Biostatistician, Complex Longitudinal Registry, Real-World Data

🔥 4 minutes ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 15%

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Serve as the statistical lead on high-profile client-facing projects • Collaborate with cross-functional teams • Design studies • Develop statistical analysis plans • Oversee statistical analyses • Provide strategic statistical leadership • Ensure high-quality and scientifically rigorous real-world evidence generation • Support consulting, pharmacovigilance, and registry coordination work within the Real-World Science department

🎯 Requirements

• Master’s degree and/or Doctorate degree in Biostatistics, Statistics, Bioinformatics, Mathematics, or a related quantitative field required • An equivalency combining appropriate education, training, and/or directly related experience may be considered sufficient • Minimum 5–8 years post-Master’s or 3–5 years post-doctorate experience in applied statistical programming in a research, pharmaceutical, biotechnology, CRO, or medical setting required • Demonstrated experience leading complex observational research studies, such as longitudinal, EMR, or registry data, required • Experience with complex longitudinal registry or real-world data required • Knowledge of retrospective and prospective observational study designs and related methodologies required • Advanced proficiency in R required • Must be legally authorized to work in the United States without sponsorship • Must pass a comprehensive background check, including drug screening • Experience mentoring or supervising junior biostatisticians preferred • Experience with SAS preferred • Strong understanding of statistical methodology for observational and longitudinal data analyses • Ability to independently lead projects, prioritize competing deliverables, and manage multiple timelines • Strong scientific, analytical, problem-solving, leadership, and communication skills • Ability to collaborate across cross-functional teams and communicate complex statistical concepts to technical and non-technical audiences • Strong attention to detail and commitment to high-quality, reproducible analyses and documentation • Excellent written communication skills and adherence to statistical programming and code documentation best practices • Ability to make independent judgments under limited supervision • Strong interpersonal and collaborative team-oriented skills

🏖️ Benefits

• Fully remote work arrangement • Standard Monday–Friday work schedule • Reasonable accommodation for disabilities during application, interview, and employment • Benefits and privileges of employment • Relocation assistance is not provided

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