Sr. Biostatistician Job at Redbock - an NES Fircroft company, Bay County, FL

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  • Redbock - an NES Fircroft company
  • Bay County, FL

Job Description

Overview

Our client is a fast-growing biotechnology company seeking a Senior Biostatistician (Associate Director level) consultant to support their Biometrics team. This role requires an experienced statistician who can function both as a study lead and as a supporting statistician, depending on project needs.

This is a hands-on role in a fast-paced biotech environment, where the successful candidate will collaborate closely with cross-functional teams and take ownership of delivering high-quality statistical support across clinical trials.

Key Responsibilities

  • Lead or support biostatistical activities for clinical trials, depending on study needs.
  • Contribute to the design, analysis, and interpretation of clinical trial data.
  • Develop and review statistical analysis plans (SAPs) and other study documentation.
  • Collaborate with cross-functional teams including Clinical Development, Data Management, Statistical Programming, and Regulatory.
  • Ensure timely delivery of statistical analyses and study outputs aligned with clinical timelines.
  • Provide statistical input for clinical study reports, regulatory submissions, and publications.
  • Participate in protocol development and study design discussions.
  • Communicate statistical concepts and results clearly to both technical and non-technical stakeholders.

Required Qualifications

  • MS in Statistics or Biostatistics and 7-8+ years of experience in pharma or biotech clinical development
  • Experience working in small biotech environments (required); preferable to have experience working both small and large sponsor organizations with strong tenure.
  • Demonstrated ability to function as both Lead Statistician and Supporting Statistician, supporting multiple clinical trials simultaneously
  • Strong experience across a variety of therapeutic areas (non-oncology)
  • Experience with placebo-controlled clinical trials
  • Strong knowledge of statistical methodologies used in clinical trials
  • Excellent written and verbal communication skills
  • Ability to operate effectively in a fast-paced, collaborative environment

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