Principal Biostatistician (FSP - Permanent Homebased)
Reading, Vereinigtes Königreich| Niederlande| Slowakei (Slowakische Republik)| Rumänien| Ungarn| Dänemark| Finnland| Deutschland| Vereinigtes Königreich| Slowenien| Spanien| Schweden| Estland| Polen| Belgien| Remote
- Full Time
- Level: Entry-level, Mid-level, Senior-level
Build a rewarding career in life sciences consulting and forge your own path. Partner with collaborative teams and leaders across unique projects and geographies, delivering innovative solutions to the most complex healthcare problems along the way. Working at IQVIA means changing outcomes for patients one data set, product offering and innovative solution at a time.
As a Consultant at IQVIA, you'll have the opportunity to grow your career and explore opportunities in brand and integrated research solutions, go-to-market strategy, commercial excellence, real world data, financial investor consulting and more.
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Principal Biostatistician (FSP - Permanent Homebased)
Stellenbeschreibung
Job Description:
The Principal Statistician will be responsible for developing and maintaining standard statistical requirements in data analysis tools and templates, ensuring compliance with industry standards and health authority regulations. These requirements will be aligned with therapeutic area needs and study design considerations.
Key Responsibilities:
- Develop and maintain standard statistical requirements, including text, definitions, and analysis requirements for Protocols and Statistical Analysis Plans.
- Create standard tables, listings, and graph mock displays with detailed analysis requirements and rules in Data Presentation Specifications.
- Maintain data analysis standards at a master level to meet scientific or operational requirements, ensuring formal change management control and versioning.
- Govern changes to standards, maintaining multiple versions to align with clinical trials and drug development programs.
- Support the clinical data standards team and standards implementation leads to ensure consistent adoption of standards in studies.
- Expertise in experimental design, modeling, analysis planning, execution, interpretation, and statistical communications support.
- Produce clear, concise, well-organized, and error-free analysis programs and statistical reporting content.
- Establish and maintain effective relationships with internal and external customers.
Educational and Experience Requirements:
- Master’s or PhD Degree in Statistics.
- Expertise in SAS or R programming.
- Working knowledge of relevant regulatory requirements (e.g., GCP, ICH) and industry standards (e.g., ADaM).
- Relevant operational experience in analysis standards is preferred.
- Experience in multiple therapeutic areas (e.g., Oncology, Cardiovascular, Immunology, Medical Devices, Neuroscience) is preferred.
- Ability to work independently with minimal oversight.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
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