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Open nowPosted 14 days ago

Director, Biostatistics FSP

Cytel38 open roles

Where
United States, Germany, United Kingdom, France
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Your applicationOpen nowDirector, Biostatistics FSPCytel · United States, Germany, United Kingdom, France

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The clock on this job

Early applications get read.

13.5% of postings close within 7 days. Measured by our own scanner across the market. Cytel postings stay open a median of 19 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.6%3 days
  3. 13.5%7 days
  4. 21.8%14 days
  5. 36.6%30 days
  6. 58.9%60 days
This job: posted 14 days ago

Cytel median: 19 days open

The posting

Job Description

Medical Affairs & HTA Statistician

Role Summary

The Medical Affairs & HTA Statistician will provide strategic and technical statistical expertise supporting evidence generation across the product lifecycle, with particular emphasis on Medical Affairs, real-world evidence, comparative effectiveness, and Health Technology Assessment.

The role will translate clinical, observational, and real-world data into scientifically robust evidence addressing questions relevant to patients, clinicians, payers, and healthcare systems. It requires a combination of strong statistical methodology, scientific judgement, strategic thinking, and effective cross-functional communication.

Responsibilities

Key Responsibilities

  • Provide statistical leadership for Medical Affairs and HTA evidence-generation activities.
  • Support development of evidence strategies addressing clinical, patient, payer, and healthcare-system questions.
  • Design and analyse observational and real-world evidence studies.
  • Apply epidemiological and statistical methodologies to real-world and clinical data.
  • Conduct comparative-effectiveness assessments and indirect treatment comparisons.
  • Support synthetic-control approaches, Phase IV studies, and other post-approval evidence-generation activities.
  • Apply appropriate HTA/HEOR methodologies and contribute statistical expertise to evidence packages supporting access and reimbursement decisions.
  • Assess data relevance and quality, quantify and communicate uncertainty, and strengthen the methodological credibility of HTA submissions and scientific discussions.
  • Interpret clinical and observational evidence and translate complex analyses into clear scientific conclusions.
  • Support publications, congress activities, and other scientific communications where required.
  • Apply modern analytical methods, including machine learning, where scientifically appropriate.
  • Collaborate with Development Statistics, Epidemiology, Real-World Evidence teams, Medical functions, and external scientific partners.
  • Communicate statistical concepts and findings effectively to cross-functional and external stakeholders.

Qualifications

Qualifications & Experience

  • Senior-level statistical/biostatistical experience within the pharmaceutical or healthcare environment.
  • Demonstrated experience delivering Medical Affairs and/or HTA statistical work packages.
  • Broad methodological expertise spanning clinical, observational, and real-world data.
  • Strong experience in one or more of: RWE, epidemiological research, comparative effectiveness, indirect treatment comparisons, synthetic controls, HTA/HEOR, or Phase IV research.
  • Strong understanding of evidence-generation strategies across the pharmaceutical product lifecycle.
  • Ability to assess data quality, methodological limitations, bias, uncertainty, and applicability of evidence.
  • Experience communicating statistical findings in publications, scientific discussions, and/or evidence packages.
  • Strong scientific judgement, strategic thinking, and stakeholder-management skills.
  • Ability to collaborate across multidisciplinary and geographically distributed teams.
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