Senior Biostatistics Leader

3 weeks ago


King of Prussia, Pennsylvania, United States Aequor Technologies Full time

Aequor Technologies is seeking a highly skilled Sr. Biostatistics Leader to lead our late phase project and regulatory submissions. The ideal candidate will have 8 years of experience with a Ph.D. or 11 years of drug development experience with an MS degree.

Job Summary:

  • Lead Regulatory Submissions: Collaborate with cross-functional teams for governance reviews, influence clinical development plans, and provide statistical thought partnership for innovative study design.
  • Statistical Strategy: Define statistical strategy, ensure appropriate methodologies applied to study design and analysis, and provide quantitative evaluation to clinical trials.
  • Communication: Prepare abstracts, posters, oral presentations, and written reports to effectively communicate results to internal and external stakeholders.

Requirements:

  • Ph.D. with 8 years of experience or MS with 11 years of drug development experience
  • Adaptive Design Experience: Hands-on skills in programming and strategic thinking required
  • Regulatory Affairs Interaction: Experience working with regulatory authorities (FDA, EMA, PMDA) necessary

Compensation: $150,000 - $200,000 per year, depending on experience



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