IQVIA
Principal Biostatistician – HTA Statistics(m/w/x)
Full-timeWith HomeofficeSenior
Frankfurt am Main
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IQIQVIA
Principal Biostatistician(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Data Science
Nejo AI Summary
Leading statistical strategy for Clinical Trial Teams (CTT) at a global clinical research provider. Independent study statistician experience in late-phase clinical trials, pharmaceutical industry experience strongly preferred. Diverse global clinical trial projects.
Requirements
- Advanced degree in Biostatistics, Statistics, or related field (PhD preferred; Master’s with significant experience)
- Proven independent study statistician experience in late-phase clinical trials
- Pharmaceutical industry experience (strongly preferred); CRO experience (plus)
- Hands-on expertise with clinical outcomes studies
- Ability to implement complex statistical methods and guide analytical decision-making
- Proficiency in SAS; working knowledge of R (advantageous)
- Regulatory submissions and health authority interaction experience (plus)
Tasks
- Lead as the primary statistician on the CTT.
- Represent Biostatistics on the CTT.
- Work independently to support clinical teams.
- Provide proactive statistical guidance.
- Lead statistical strategy discussions.
- Define study endpoints and analysis methods.
- Address risk mitigation and regulatory expectations.
- Independently author Statistical Analysis Plans (SAPs).
- Conduct complex time-to-event analyses.
- Apply MMRM and longitudinal models.
- Utilize estimand-aligned statistical methods.
- Perform and oversee statistical analyses.
- Conduct sample size calculations using SAS or R.
- Justify design assumptions to clinical leadership.
- Collaborate with statistical programmers.
- Provide clear direction to programmers.
- Review statistical programming outputs.
- Ensure SAP and programming alignment.
- Perform hands-on SAS programming for clinical datasets.
- Actively participate in CTT meetings.
- Drive alignment across cross-functional teams.
- Communicate proactively with team members.
- Anticipate team needs and address issues.
- Ensure clarity on statistical approaches.
- Explain statistical concepts to non-statistical stakeholders.
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS
- R
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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IQIQVIA
Principal Biostatistician(m/w/x)
Frankfurt am Main
Full-timeWith Home OfficeSenior
Data Science
Nejo AI Summary
Leading statistical strategy for Clinical Trial Teams (CTT) at a global clinical research provider. Independent study statistician experience in late-phase clinical trials, pharmaceutical industry experience strongly preferred. Diverse global clinical trial projects.
Requirements
- Advanced degree in Biostatistics, Statistics, or related field (PhD preferred; Master’s with significant experience)
- Proven independent study statistician experience in late-phase clinical trials
- Pharmaceutical industry experience (strongly preferred); CRO experience (plus)
- Hands-on expertise with clinical outcomes studies
- Ability to implement complex statistical methods and guide analytical decision-making
- Proficiency in SAS; working knowledge of R (advantageous)
- Regulatory submissions and health authority interaction experience (plus)
Tasks
- Lead as the primary statistician on the CTT.
- Represent Biostatistics on the CTT.
- Work independently to support clinical teams.
- Provide proactive statistical guidance.
- Lead statistical strategy discussions.
- Define study endpoints and analysis methods.
- Address risk mitigation and regulatory expectations.
- Independently author Statistical Analysis Plans (SAPs).
- Conduct complex time-to-event analyses.
- Apply MMRM and longitudinal models.
- Utilize estimand-aligned statistical methods.
- Perform and oversee statistical analyses.
- Conduct sample size calculations using SAS or R.
- Justify design assumptions to clinical leadership.
- Collaborate with statistical programmers.
- Provide clear direction to programmers.
- Review statistical programming outputs.
- Ensure SAP and programming alignment.
- Perform hands-on SAS programming for clinical datasets.
- Actively participate in CTT meetings.
- Drive alignment across cross-functional teams.
- Communicate proactively with team members.
- Anticipate team needs and address issues.
- Ensure clarity on statistical approaches.
- Explain statistical concepts to non-statistical stakeholders.
Work Experience
- approx. 4 - 6 years
Education
- Master's degree
Languages
- English – Business Fluent
Tools & Technologies
- SAS
- R
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of IQVIA and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
IQVIA
Industry
Healthcare
Description
IQVIA is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients.
Not a perfect match?
- IQVIA
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