Principal Biostatistician - Safety (FSP)
At a glance
Senior Data Science role at Thermofisher. Remote, Belgium · full-time.
Pay not stated Data Science salary
remoteroles summary, based on the employer's posting.
What you'll do
- Apply statistical methods across clinical trials, from shaping study designs and protocols through final analyses and reports
- Develop and review statistical analysis plans for clinical research studies
- Produce safety and benefit-risk analyses, including DSUR and PSUR reporting and post-marketing work
- Coordinate statistical work across several clinical trials at once
What you bring
- An advanced degree plus six years of relevant experience, or a bachelor’s degree plus eight years, in clinical research biostatistics
- Expert SAS programming ability and strong command of statistical methods
- Experience developing or reviewing analysis plans, and working with safety reporting and benefit-risk assessments
- Working knowledge of ICH-GCP, trial regulations and CDISC standards
Who this fits
This role suits a senior biostatistician with clinical trial experience, particularly across Phase I to III studies. You’ll work closely with clients in an FSP position, supporting studies from design through reporting.
From the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.
About the Opportunity
You will have the opportunity to support an innovative, science-driven global biotechnology company focused on developing transformative therapies for people living with severe autoimmune diseases.
Working in a dynamic and collaborative environment, you will contribute to a growing portfolio of clinical research programmes, helping generate the scientific evidence needed to better understand treatments and improve patient outcomes.
This is an exciting opportunity to apply your statistical expertise within a highly innovative therapeutic area, collaborate with leading scientific experts and play a key role in advancing research with the potential to make a meaningful difference in patients' lives.
DESCRIPTION:
Join our Clinical Research team as a Principal Scientist in Biostatistics, where you'll contribute to advancing life-changing therapies through statistical excellence. As part of our Functional Service Provider (FSP) division, you'll work closely with clients while utilizing the benefits and resources of an established leader in clinical research. You'll be responsible for implementing diverse statistical tasks throughout the full clinical trial process, from study design and protocol writing to final analysis and reporting. This position offers the opportunity to impact health outcomes while working with advanced clinical development programs.
REQUIREMENTS:
• Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of experience in biostatistical experience in clinical research, with emphasis on Phase I-III trials
• Preferred Fields of Study: Statistics, Biostatistics, or related quantitative field
• Expert-level proficiency in SAS programming and statistical methodology
• Strong knowledge of ICH-GCP guidelines and clinical trial regulations
• Demonstrated experience in statistical analysis plan development and review
• Demonstrated experience in Benefit-risk analysis, Safety reporting DSUR, PSUR; Post-marketing analysis, MA, RWE, claims database
• Ability to manage multiple clinical trials simultaneously
• Advanced knowledge of CDISC standards and their implementation
• Experience with statistical software packages such as R, EAST, or WinBUGS
• Strong analytical and problem-solving skills
• Excellence in written and verbal communication
• Ability to interact effectively with regulatory authorities (FDA, EMA)
• Experience in CRO environment and vendor management preferred
• Knowledge of auto-immune and/or oncology therapeutic areas beneficial
• Demonstrated ability to work collaboratively in teams
• Ability to meet deadlines and manage competing priorities
• Strong attention to detail and quality focus
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