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BeOne Medicines

Associate Director, Biostatistics

BeOne Medicines

Statistician providing statistical solutions for EU HTA requirements and collaborating with cross-functional teams. Focused on evidence generation and modeling to meet organizational needs.

Posted 6/12/2026full-time🇨🇭 SwitzerlandSenior💰 CHF 164,100 - CHF 205,100 per yearWebsite

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
statistical analysis methodologiesexperimental designeconomic modelingindirect comparisonsobservational studiesdata analysisstatistical programmingplanning clinical trialsanalysis of clinical trialsreporting clinical trials
Soft Skills
presentation skillsoral communicationwritten communicationproactivemotivatedattention to detailteam collaborationproblem-solvingtrainingstrategic thinking
Tools & Technologies
SASR
Certifications & Qualifications
PhD in StatisticsPhD in BiostatisticsMaster’s degree in StatisticsMaster’s degree in Biostatistics
Industry Keywords
HTAJCAEU submissionscross-functional teamsclinical trial designdrug development processevidence generationvendor-supplied datalocal HTA adaptationsstatistical subject matter expert

About the role

Key responsibilities & impact
  • Close collaboration with cross-functional teams to support the quantitative needs for HTA submissions in Europe
  • Provide strategic statistical input into evidence generation activities and analyses required for the EU JCA
  • Provide quantitative support for local HTA adaptations
  • Influence and shape new ways of working to ensure organizational readiness to successfully meet the needs of the EU JCA
  • Serve as a subject matter expert in relevant EU cross-functional teams
  • Collaborate with HEOR and external vendors to build models in support of EU submissions with a focus on HTA/JCA analysis.
  • Attend advisory board meetings and internal strategic meetings and provide statistical analysis input.
  • Work with the statistical programming staff to ensure that all programs meet internal and external analysis requirements.
  • Contribute significantly in providing key and innovative ways to data analyses, including the interpretation of results and the presentation to leadership of findings.
  • Keep up to date with respect to statistical methodology in HTA and use efficient or innovative approaches in economic modeling, indirect comparisons, and observational studies.
  • Identify and anticipate technical or other potential problems arising in the design, conduct, and analysis of studies, and be able to propose and implement solutions.
  • Serve as the statistical subject matter expert in cross-functional teams.
  • Contribute to creation/maintenance of, and provide training on, statistical topics and departmental SOPs, work instructions, etc.
  • Provide quantitative support to address the needs for local adaptations and adhoc HTA requests.
  • Ensure consistency and adherence to standards across compounds and/or therapeutic areas.
  • Review vendor-supplied data and analysis as needed.

Requirements

What you’ll need
  • PhD or equivalent degree in Statistics/Biostatistics or related discipline with a minimum of 5 years relevant work experience, or a Master’s degree with a minimum of 7 years relevant work experience.
  • Significant experience in HTA in Europe and other major markets.
  • Solid knowledge of statistical analysis methodologies and experimental design.
  • Proficient in statistical and data processing software such as SAS and R.
  • Good presentation, oral and written communication skills in English.
  • Ability to learn, be proactive, motivated, and consistently focus on details and execution.
  • Strong interest in statistical research activities and application of novel methods to clinical trial development.
  • Ability to work in a team environment with multiple cross-functional team members.
  • Knowledge of clinical trial design concepts; in-depth knowledge of all phases of the drug development process.
  • Demonstrated skills in the planning, analysis and reporting of clinical trials.

Benefits

Comp & perks
  • Health insurance
  • 401(k) matching
  • Flexible work hours
  • Paid time off
  • Professional development opportunities