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.
- Develop and implement novel statistical methods to tackle complex challenges.
- Address market access and reimbursement challenges from regional agencies via cross-functional collaboration.
- Work with Health Outcomes and Market Access teams to analyze and interpret clinical trials and real-world data.
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 in late-phase clinical drug development.
- Programming skills in R and/or Python.
- Self-motivated with strong time management to manage multiple projects.
- Excellent interpersonal/communication skills, including explaining methods to senior stakeholders.
- Experience influencing across functions and organizational levels.
Preferred Qualifications & Skills:
- Statistical contributions in medical affairs/market access (including HTA assessment).
- Experience in oncology.
- Leadership/major contributions to organizational or industry initiatives.
- Innovative statistical thinking.
- Teamwork/relationship building.
- Experience coordinating work with CROs.
Application instructions:
- Apply using the online application cover letter or your CV to describe how you meet the competencies.
- Closing date for applications: 7th May.