A well-established, secure and commercially active biopharma is expanding its US biostatistics team. This is a therapeutically-aligned role focused on statistical analysis across an oncology portfolio.
Responsibilities
In support of the Associate Director, Biostatistics, work on clinical data for the company's Oncology portfolio
Help develop and review analysis plans and statistical sections of study protocols
Collaborate with clinical development, translational science, and biometrics teams
Support regulatory interactions and contribute to clinical study reports
Conduct ad hoc statistical analysis as required
Experience Required
PhD in Biostatistics or Statistics; Masters with supplementary experience considered
Strong oncology experience
Demonstrable experience working directly for a sponsor company
Proficiency in SAS and/or R
Understanding of biomarker endpoints and translational study designs would be of benefit, but not required
East Coast based only
Compensation DOE - $140,000 - $180,000 base salary + benefits
Numbers & Facts
Location
(Remote)
Skills
Biomarkersunmatched
Biometricsunmatched
Biostatisticsunmatched
Clinical Dataunmatched
Clinical Trialunmatched
Drug Developmentunmatched
Oncologyunmatched
R Programming Languageunmatched
Regulationsunmatched
Research Protocolsunmatched
Statisticsunmatched
Translational Researchunmatched
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