Senior Biostatistician (complex longitudinal registry or real-world data required)

Overview

The Senior Biostatistician serves as the statistical lead on high-profile client-facing real-world evidence projects, working collaboratively with cross-functional teams.

What you'll do

• Design studies and develop statistical analysis plans.
• Oversee analyses to ensure high-quality, scientifically rigorous real-world evidence generation.
• Provide strategic statistical leadership across consulting work, pharmacovigilance, and registry coordination.

What you'll need

• 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 will be considered.
• Minimum 5–8 years post Master's or 3-5 years post-doctorate applied statistical programming experience in a research, pharmaceutical, biotechnology, CRO, or medical setting required.
• Demonstrated experience leading complex observational research studies (e.g. longitudinal, EMR, 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.
• 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 effectively 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.

Nice to have

• Experience mentoring or supervising junior biostatisticians.
• Experience with SAS.

Details

• Location: Remote in the United States.
• Standard work schedule Monday through Friday.
• Relocation assistance is not provided.
• Must be legally authorized to work in the US without sponsorship.
• Must be able to pass a comprehensive background check, including a drug screening.