Director of Statistical Excellence
1 month ago
We are seeking a highly skilled and experienced Director-level professional to join our team as a Statistics Director. This is a key leadership position that will play a critical role in driving statistical excellence and strategic influence on clinical development plans for our vaccine projects.
Key Responsibilities- Lead the statistical input to project development teams, driving innovation and ensuring commitment to quality standards, processes, and efficient delivery.
- Contribute to strategic planning and quantitative decision-making.
- Foster a culture of innovation and act as a role model to others in actively owning and driving the use of innovative methods where appropriate.
- Provide statistical leadership within the clinical statistics department and R&D organization.
- Provide statistical input to the design, analysis, reporting, and interpretation of clinical studies.
- Provide statistical contributions and strategic input to clinical development plans.
- Provide leadership on regulatory strategy.
- Build and maintain effective strategic working relationships with internal and external partners to deliver on business needs.
- Interact effectively with key stakeholders and governance boards.
- MSc or PhD in a Statistical discipline with 10+ years of experience in the biotech or pharmaceutical industry.
- Minimum three years of experience in line management of a team of statisticians, including objective setting and performance reviews.
- Experience with innovation and applying cutting-edge approaches in drug or vaccine development.
- Proven interpersonal and communication skills, including experience maintaining strong working relationships, explaining novel and standard methods to scientific and clinical senior stakeholders, and influencing across functions and levels of an organization.
- Strong time-management skills, able to effectively organize and manage a variety of tasks across different projects.
- Track record of strong statistical contributions and accomplishments in clinical development, with a broad knowledge of all phases of drug development (pre-clinical; Phase I-IV).
- Demonstrated ability to lead or make major contributions to department, organizational, and/or industry-wide initiatives, through effective communication and influence.
- Expertise in a range of statistical methodologies with application to real problems.
- Examples of applying innovative statistical thinking.
- Experience with Bayesian methods.
- Experience across a wide range of therapeutic areas.
- Self-motivated and independent worker.
- Experience of working with and coordinating the work of CROs.
- Experience working on regulatory submissions.
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