Statistics Leader/Associate Director

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares and savings programme. We embrace modern work practices; our Performance with Choice programme offers a hybrid working model, empowering you to find the optimal balance between remote and in-office work.

This role can be based in Stevenage, UK, London, UK, Waltham, US, Collegeville, US, or remotely. We are seeking a skilled Statistics Leader or Associate Director to play a key role in supporting marketed products and advancing new cancer treatments. In this position, you will provide global statistical expertise for various initiatives, including non-registrational data generation, Phase IV studies, secondary publications, scientific congress support, and ISR review. These efforts will help deliver clearly differentiated medicines to patients. You will work closely with teams across R&D, medical, and commercial organizations, as well as with Real-World Evidence (RWE) and Health Outcomes Research groups, to manage a diverse portfolio of projects that support market access for GSK oncology products and late-stage pipeline assets.

In this role you will…

• Provide statistical expertise for non-registrational studies, including design, analysis, reporting, and interpretation, while influencing clinical development, regulatory, and commercial strategies.
• Collaborate with internal and external partners to meet business needs, including reviewing Investigator Sponsored Research (ISR) and GSK-sponsored Phase IV trials.
• Develop and apply novel statistical methodologies to address challenges in market access and reimbursement, partnering with global and regional teams.
• Work with Health Outcomes and Market Access teams to analyze and interpret real-world data, such as patient registries and claims databases.
• Address market access challenges posed by regional agencies (e.g., NICE, IQWiG, HAS, PBAC) through collaboration with cross-functional teams.
• Formulate data strategies to leverage internal and external databases for R&D oncology and invest in expanding expertise across clinical, regulatory, and commercial domains.

Basic Qualifications & Skills:

• MSc or equivalent degree in a Statistical discipline.
• Relevant experience from clinical research, pharmaceutical, CRO or academia.
• Track record of strong statistical contributions and accomplishments in late phase clinical drug development.
• Proficient in both spoken and written English, with the capability to clearly communicate both new and established statistical methods and results based on those methods to peers without substantial statistical training.

Preferred Requirements:

• PhD degree in a Statistical discipline.
• Oncology experience.
• Track record of strong statistical contributions and accomplishments in medical affairs and market access of marketed products.
• Demonstrated ability to lead or make major contributions to department, organizational and/or industry-wide initiatives, through effective communication and influence.
• Excellent interpersonal and communication skills. Capability in building and maintaining strong working relationships in a team setting.
• Experience of working with and coordinating the work of others.

Closing Date for Applications – Wednesday 2nd of April (COB)

As an Equal Opportunity Employer, we are open to all talent. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.