Thermo Fisher Scientific develops and delivers technologies, laboratory products, and pharmaceutical services that support scientific research and healthcare. Its work spans life sciences research, analytical problem-solving, laboratory productivity, diagnostics, and the development and manufacturing of therapies. The company serves customers through a global team and a portfolio of brands including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Its careers encompass the scientific, healthcare, manufacturing, logistics, and service operations behind these offerings.
Principal Biostatistician, Clinical Research
Lead statistical work across Thermo Fisher Scientific clinical research programs, from study design and protocol development through final analysis and reporting. Apply SAS, CDISC standards, and statistical methods to Phase I–III trials.
Description
- Apply statistical expertise to support the development of life-changing therapies.
- Join the Clinical Research team in Thermo Fisher Scientific’s Functional Service Provider division.
- Partner with clients while drawing on the resources of an established clinical research organization.
- Carry out statistical work across all stages of the clinical trial process.
- Help shape study designs and write protocols.
- Complete final analyses and prepare reports.
- Support advanced clinical development programs and contribute to improved health outcomes.
Requirements
- Advanced degree and at least 6 years of clinical research biostatistics experience, or a bachelor’s degree and at least 8 years; experience with Phase I–III trials is emphasized.
- Preferred education in statistics, biostatistics, or a related quantitative discipline.
- Expert proficiency in SAS programming and statistical methods.
- Strong understanding of ICH-GCP guidance and clinical trial regulations.
- Experience developing and reviewing statistical analysis plans.
- Ability to oversee several clinical trials at the same time.
- Advanced understanding of CDISC standards and their application.
- Experience with statistical tools such as R, EAST, or WinBUGS.
- Strong analytical reasoning and problem-solving abilities.
- Excellent written and spoken communication skills.
- Ability to work effectively with regulatory agencies, including the FDA and EMA.
- CRO and vendor management experience is preferred.
- Familiarity with autoimmune or oncology therapeutic areas is beneficial.
- Ability to collaborate effectively with colleagues.
- Ability to meet deadlines while balancing competing priorities.
- Careful attention to detail and a strong focus on quality.
Benefits
- Fully remote work arrangement.
- Standard Monday-to-Friday schedule.