In this role you will…
- Provide statistical input for the design, analysis, reporting, and interpretation of non-registrational studies.
- Shape clinical development plans, HTA strategies, and commercial approaches.
- Build and maintain strategic relationships with internal and external stakeholders to address business needs.
- Develop and implement novel statistical methods to tackle complex challenges.
- Address market access and reimbursement challenges from regional agencies by collaborating with cross-functional teams.
- Work with Health Outcomes and Market Access teams to analyze and interpret clinical trials and real-world data, while expanding expertise beyond traditional statistics.
Basic Qualifications & Skills (required):
- MSc or PhD in Statistics, Mathematics or equivalent with relevant experience in clinical research, pharmaceutical, CRO, or academic settings.
- Proven statistical contributions and accomplishments in late-phase clinical drug development.
- Good statistics programming skills and experience in R and/or Python.
- Self-motivated with strong time management skills to manage multiple tasks across projects.
- Excellent interpersonal and communication skills, including explaining methods to senior stakeholders.
- Experience influencing across functions and organizational levels.
Preferred Qualifications & Skills:
- Proven statistical contributions in medical affairs and market access for marketed products, including HTA assessment.
- Experience in oncology.
- Demonstrated leadership and major contributions to organizational or industry-wide initiatives.
- Ability to apply innovative statistical thinking.
- Strong relationship-building and teamwork skills.
- Experience coordinating work with CROs.
Application instructions:
- Closing Date for Applications: 7th May.
- Use the online application ‘cover letter’ or your CV to describe how you meet the competencies for this role.