Principal Biostatistician - Medical Affairs (FSP)
Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every day, enabling our customers to make the world healthier, cleaner and safer. We empower our global teams with the resources and opportunities needed to achieve their individual career goals while advancing science through innovative solutions to some of the world's most complex challenges. From protecting the environment and ensuring food safety to supporting the discovery of life-changing cancer treatments, our work makes a meaningful difference.
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.
Key Responsibilities
As part of the Medical Affairs Statistics team, you will provide strategic statistical expertise and oversight across clinical research programmes, with a particular focus on Phase IIIb/IV clinical trials, observational studies and patient registries supporting post-marketing commitments and requirements.
You will serve as a key statistical representative within cross-functional teams, providing scientific leadership while managing multiple studies and projects simultaneously.
Clinical Study Design and Statistical Leadership
- Provide statistical expertise and oversight for clinical trials, observational studies, patient...
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