Experts who apply statistical methods to biological and medical data. Essential for clinical trials and research studies, biostatisticians ensure the validity and reliability of scientific findings.
Biostatisticians play a crucial role in the biotechnology sector by applying statistical methods to biological and medical data. They are vital for the design, analysis, and interpretation of clinical trials and research studies, ensuring that scientific findings are both valid and reliable. Biostatisticians work across a range of organisations, from pharmaceutical companies and research institutions to government agencies and healthcare providers, contributing to the development of new treatments and the advancement of medical knowledge.
A typical week for a biostatistician is a mix of data analysis, project management, and collaboration with cross-functional teams.
% of 2 listings posted in the last 12 months that mention each skill, extracted from job descriptions.
A typical UK progression for biostatisticians. Years are guidance — strong people move faster, and many senior folks sidestep into research, product or management.
Assists in data collection, cleaning, and basic statistical analysis. Works under the supervision of senior biostatisticians.
Leads the design and analysis of clinical trials. Manages data quality and integrity. Collaborates with multidisciplinary teams.
Oversees multiple projects and provides expert statistical advice. Develops and implements advanced statistical methods.
Strategic leader in biostatistics. Influences company-wide statistical policies and practices. Mentors and develops junior staff.
There's no single route, but most people follow some version of these steps.
Earn a degree in statistics, biostatistics, or a related field. Gain a strong foundation in statistical theory and methods.
Start as a Junior Biostatistician, working on data collection and basic analysis under supervision.
Develop expertise in clinical trial design and data analysis. Take on more complex projects and responsibilities.
Move into senior positions, leading teams and projects. Provide strategic guidance and mentor junior staff.
Focus on a specific area such as genomics, bioinformatics, or regulatory affairs. Become a recognised expert in your field.
Advance to executive roles, influencing company-wide policies and practices. Lead major initiatives and drive innovation.
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This role involves leading the development and delivery of strategic life sciences partnerships for the South West Secure Data Environment (SWSDE). Responsibilities include building relationships with life science organizations, developing commercial models, and ensuring governance and ethical standards are maintained.
This role involves building and maintaining scalable data services and platforms that support AI-driven drug discovery. You'll work closely with scientists and ML researchers to ingest, transform, and serve complex scientific data, enabling high-velocity research. The position requires strong backend engineering skills, particularly in Python and GCP, within a collaborative, interdisciplinary environment.
This role involves leading pharmacovigilance and risk management strategy for GSK's global assets, with a focus on safety evaluation in immunology and other therapeutic areas. The Scientific Director will lead safety governance, contribute to regulatory submissions, and manage cross-functional teams to address product safety issues. They will also represent GSK in interactions with regulatory authorities and ensure compliance with global pharmacovigilance standards.
This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation in immunology and other therapeutic areas. The Scientific Director will oversee safety governance, lead cross-functional teams, and ensure compliance with global regulations. They will analyze clinical data, manage safety issues, and contribute to regulatory submissions and long-term clinical strategy.
This role involves leading pharmacovigilance and risk management strategies for GSK's global assets, with a focus on safety evaluation and benefit-risk management across clinical development and post-marketing settings. The position requires expert analysis of clinical and safety data, leadership in cross-functional governance teams, and strategic input into regulatory submissions and risk mitigation. It plays a critical part in ensuring patient safety and regulatory compliance within immunology and other therapeutic areas.
This role involves leading pharmacovigilance and risk management strategies for GSK’s global assets, with a focus on immunology. The Scientific Director will evaluate safety data, lead cross-functional teams, and ensure compliance in clinical development and post-marketing settings. The position requires deep expertise in safety evaluation, signal detection, and international regulatory standards.
A degree in statistics, biostatistics, or a related field is essential. Advanced degrees and relevant certifications can enhance your career prospects.
Commonly used software includes R, SAS, and Python. Familiarity with these tools is crucial for data analysis and statistical modelling.
Collaboration is vital. Biostatisticians work closely with researchers, clinicians, and other scientists to design studies and interpret data.
Salaries vary based on experience and location. For specific salary ranges, please refer to the salary section on this page.
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