Responsibilities
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
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.
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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
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.
#J-18808-Ljbffr
Associate Director, Biostatistics Arbeitgeber: Jobtailor
Als Global Director B2B – Business Development bei uns profitieren Sie von einer dynamischen und innovativen Arbeitsumgebung, die auf Zusammenarbeit und Kreativität setzt. Wir bieten Ihnen nicht nur attraktive Vergütungsmodelle und umfassende Weiterbildungsmöglichkeiten, sondern auch die Chance, in einem internationalen Team zu arbeiten, das Vielfalt und persönliche Entwicklung fördert. Unsere Unternehmenskultur legt großen Wert auf Flexibilität und Work-Life-Balance, sodass Sie Ihre Karriereziele in einem unterstützenden Umfeld erreichen können.
