Real World Principal Biostatistician (Biostatistics)
Контакты
Формат работы
hybrid/onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
UK/Germany
rstatistical analysissasbiostatisticsclinical trialsreal world evidenceobservational studies
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В Vertex четко описана опытная роль в биостатистике с задачами для клинических и real-world исследований; зарплата не указана, поэтому уровень компенсации оценить сложно.
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TL;DR
Real World Principal Biostatistician (Biostatistics): Performing advanced statistical analyses for clinical trials, real-world observational studies, market access, and post-marketing drug development with an accent on study design, statistical analysis plans, and cross-functional evidence generation. Focus on developing sample size estimates and randomization plans, reviewing TFLs, guiding statistical programming, and communicating results to regulators, payers, and scientific stakeholders.
Location: Paddington, United Kingdom; other location: Munich, Germany. Hybrid work is available remotely up to two days per week, or the role may be performed on-site five days per week.
Company
Vertex is a global biotechnology company focused on scientific innovation and the development of medicines.
What you will do
Lead advanced statistical work for clinical trials, observational studies, and real-world data investigations.
Develop study protocols, sample size estimates, randomization plans, Statistical Analysis Plans, and TFL shells.
Prepare data review plans, key results memos, dissemination plans, clinical study reports, publications, and posters.
Provide strategic statistical guidance and collaborate with Clinical Development, Medical Affairs, Health Economics and Outcome Research, Real World Evidence, and programming teams.
Represent Statistics in Study Execution Team meetings and Statistical Review Forum discussions.
Contribute to regulatory, payer, review board, and departmental working group interactions.
Requirements
Ph.D. in Biostatistics or a related field with 3 years of relevant experience, or an M.S. in Biostatistics with 6 years of relevant experience.
Advanced understanding of statistical methods used in drug development and post-marketing research.
Competence with SAS and R statistical software.
Strong critical thinking, logical problem-solving, written communication, and verbal communication skills.
Ability to collaborate effectively with statisticians, non-statisticians, and multiple cross-functional stakeholders.
Culture & Benefits
Hybrid or on-site work designation under the Flex @ Vertex program.
Continuous learning focused on AI, technology, automation, and industry trends.
Equal employment opportunity and reasonable accommodations for qualified applicants.
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