Senior Biostatistician – Complex Longitudinal Registry, Real-World Data

🕒 September 2

🌲 North Carolina – Remote

🌲 North Carolina – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 28%

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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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Serve as the statistical lead on high-profile, client-facing projects • Work collaboratively with cross-functional teams • Design studies • Develop statistical analysis plans • Oversee analyses • Provide strategic statistical leadership • Ensure high-quality and scientifically rigorous real-world evidence generation • Support consulting work, pharmacovigilance, and registry coordination 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 consisting of a combination of 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 of applied statistical programming experience 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 working with complex longitudinal registry or real-world data required • Demonstrated knowledge of retrospective and prospective observational study designs and related methodologies required • Advanced proficiency in R required • 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 effectively • Strong scientific, analytical, problem-solving, leadership, and communication skills • Demonstrated 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 best practices for statistical programming and code documentation • Ability to make independent judgments under limited supervision • Strong interpersonal skills and a collaborative team-oriented mindset • Must be legally authorized to work in the US without sponsorship • Must be able to pass a comprehensive background check, including a drug screening

🏖️ Benefits

• Relocation assistance is NOT provided • Equal employment opportunity and affirmative action employer • Reasonable accommodation for individuals with disabilities • Accessibility service for job seekers requiring accommodations • Standard Monday–Friday work schedule