Senior Biostatistician

Job not on LinkedIn

🔥 0 minutes ago

🌲 North Carolina – Remote

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⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

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Logo of Thermo Fisher Scientific

Thermo Fisher Scientific

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 data/programming lead for complex studies and contribute in a client-facing capacity • Lead all data/programming aspects for complex studies end-to-end • Independently present results and handle client questions related to data and output • Act as technical lead and study-level owner • Independently oversee analyses and provide strategic programmatic leadership • Ensure high-quality and scientifically rigorous real-world evidence generation • Lead database design input, CRF structure, and data validation strategy • Collaborate across cross-functional teams and communicate statistical concepts to technical and non-technical audiences • Produce reproducible analyses and documentation following statistical programming best practices

🎯 Requirements

• Master’s degree and/or Doctorate degree in Biostatistics, Statistics, Bioinformatics, Mathematics, or a related quantitative field required • 3–5 years of applied statistical programming experience using SAS and R in a research, pharmaceutical, biotechnology, CRO, or medical setting required • Demonstrated experience leading complex observational research studies, such as longitudinal, EMR, or registry data studies • Experience working with complex longitudinal registry or real-world data • Demonstrated knowledge of retrospective and prospective observational study designs and related methodologies • Advanced proficiency in R required • Experience with SAS required • Experience leading database design input, CRF structure, and data validation strategy • 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, communication, written communication, interpersonal, and collaboration skills • Ability to communicate complex statistical concepts to technical and non-technical audiences • Strong attention to detail and commitment to high-quality, reproducible analyses and documentation • Ability to make independent judgments under limited supervision • Experience mentoring or supervising junior biostatisticians preferred

🏖️ Benefits

• Fully remote work arrangement • Accessibility accommodations for the job application or interview process and essential job functions

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