
Senior Biostatistician – Complex Longitudinal Registry, Real-World Data
Posted Sep 2

Posted Sep 2
This is a fully remote position, open to applicants in North Carolina.
• Act as the statistical lead on prominent client-facing initiatives
• Work collaboratively with cross-functional teams
• Design research studies
• Create statistical analysis plans
• Supervise analytical processes
• Offer strategic statistical guidance for the generation of high-quality, scientifically sound real-world evidence
• Assist with consulting tasks, pharmacovigilance, and registry management within the Real-World Science department
• A Master’s degree and/or a Doctorate degree in Biostatistics, Statistics, Bioinformatics, Mathematics, or a related quantitative discipline is required
• An equivalent combination of relevant education, training, and/or directly related experience may be deemed adequate
• At least 5–8 years of post-Master’s or 3–5 years of post-doctorate experience in applied statistical programming within a research, pharmaceutical, biotechnology, CRO, or medical environment is required
• Proven experience in leading complex observational research studies, such as longitudinal, EMR, or registry data, is necessary
• Experience with intricate longitudinal registry or real-world data is required
• In-depth knowledge of retrospective and prospective observational study designs and associated methodologies is essential
• Advanced proficiency in R is mandatory
• A solid understanding of statistical methodologies for observational and longitudinal data analyses is required
• Ability to independently manage projects, prioritize competing deadlines, and handle multiple timelines
• Strong scientific, analytical, problem-solving, leadership, and communication skills
• Capability to collaborate with cross-functional teams and convey complex statistical ideas to both technical and non-technical audiences
• Exceptional attention to detail and dedication to producing high-quality, reproducible analyses and documentation
• Excellent written communication skills and commitment to best practices in statistical programming and code documentation
• Ability to make independent decisions with minimal supervision
• Strong interpersonal skills and a team-oriented approach
• Must possess legal authorization to work in the US without sponsorship
• Must successfully pass a comprehensive background check, including a drug screening
• Fully remote work arrangement
• Reasonable accommodations available for individuals with disabilities
• Additional benefits and employment privileges
Abbott
Amgen
Abbott
Tempus AI
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