Biostatistician I - Dermatology
About The Position
The Biostatistician I provides statistical support for clinical projects, including study design, sample size determination, and protocol development. The role prepares statistical analysis plans, generates statistical summary tables, and integrates databases to enable more comprehensive analyses. It also performs and interprets statistical analyses, documents and communicates findings, and contributes statistical methods and text to reports, publications, abstracts, manuscripts, and grant applications. The position works with principal investigators, sponsors, external representatives, clinical research teams, and statistical programmers to support accurate, unbiased project results and meet project objectives and timelines. It helps identify and resolve potential data issues, reviews analysis plans for consistency with study protocols, and follows departmental standard operating procedures for documentation and validation of clinical research statistics.
Requirements
- Master’s degree in biostatistics, computational biology, or a related field.
- Advanced-level experience with SAS, R, or a similar application.
Nice To Haves
- 1–2 years of biostatistics or related experience in clinical research.
Responsibilities
- Prepare statistical analysis plans and timelines for statistical project management.
- Perform and interpret basic and complex analyses, proposing additional analyses when appropriate based on statistical knowledge and medical understanding.
- Document analyses, create summaries, and present written and verbal results to requestors.
- Write statistical text for study reports and clinical publications, and prepare analysis plans and methods for abstracts, manuscripts, and grants.
- Identify potential data problems from analytic queries and take appropriate actions to guide their resolution.
- Collaborate with principal investigators, sponsors, and external representatives to ensure results and conclusions are presented accurately and without bias, and to achieve project objectives and timelines.
- Review statistical analysis plans for consistency with protocols and adequacy in meeting protocol objectives.
- Follow functional department standard operating procedures for documentation and validation of clinical research statistics.
- Consult with clinical research project teams on statistical issues related to projects.
- Collaborate with statistical programmers supporting clinical projects to identify and resolve potential data problems.
- Perform other related duties.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
