Principal Statistician - Stevenage, United Kingdom - GlaxoSmithKline

Description

Site Name: USA - Pennsylvania - Upper Providence, GSK House, UK - Hertfordshire - Stevenage

Posted Date: Mar

Medical & Market Access Principal Statistician - US / UK / Remote

GSK Oncology has a commitment to the discovery and development of new oncology therapies with the life-changing potential of helping patients with cancer, specifically in four areas of cancer research: Cancer Epigenetics, Immuno-Oncology, Oncology Cell & Gene Therapy and Synthetic Lethality.

We need exceptionally talented and committed Statisticians to apply statistical skills and innovative statistical methodology to drive key contributions in the marketed product support of new medicines in the fight against cancer. You will provide global statistical support in non-registrational data generation, secondary publications and scientific congress support, and ISR review to support delivery of clearly differentiated medicines to our patients. You will also collaborate with R&D, medical and commercial organizations as well as Value Evidence & Outcomes teams to deliver a diverse stream of work to support evidence generation for market access of GSK marketed oncology products and late stage pipeline assets. Join our team of industry leading experts in data analysis and methodologic research. Our end-to-end project support model ensures that our Statisticians have opportunities to collaborate across the entire range of drug development, from early clinical development, to registration and marketed product support.

US Hiring Locations: Collegeville, PA and Waltham, MA

UK Hiring Locations: Stevenage, GSK House

Remote Working: Available

Details:

• Providing statistical input to the design, analysis, reporting and interpretation of non-registrational studies.
• Influencing clinical development plans, regulatory and commercial strategies.
• Building and maintaining effective strategic working relationships with internal and external partners to meet business needs.
• Identifying, developing and implementing novel statistical methodologies.
• Addressing challenges in market access and reimbursement raised by regional agencies such as the Institute for Quality and Efficiency in Health Care (IQWiG) and Federal Joint Committee (G-BA) in Germany, UK National Institute for Health and Clinical Excellence (NICE), France Haute Autorit? de Sant? (HAS) and Australia Pharmaceutical Benefits Advisory Committee (PBAC), in collaboration with other functions
• Collaborating with global/regional Health Economics and Market Access Teams on identifying analysis methods and interpretation of observation data and other real-world type data (such as Patient Registries and Claims Databases).
• Investing in developing knowledge outside of conventional statistical expertise in the clinical, regulatory and commercial environments.

Why You?

Basic Qualifications:

• MSc or PhD in a Statistical discipline with relevant experience in a clinical research, Pharmaceutical, CRO or Academic setting.

Preferred Qualifications:

• Track record of strong statistical contributions and accomplishments in medical affairs and market access of marketed products.
• Track record of strong statistical contributions and accomplishments in late phase clinical drug development
• Self-motivated and independent worker.
• Strong time management skills; able to effectively organize and manage a variety of tasks across different projects.
• Excellent interpersonal and communication skill, including:
• Demonstrated ability building and maintaining strong working relationships.
• Ability to explain novel and standard methods to scientific and clinical senior stakeholders.
• Experience successfully influencing effectively across functions and levels of an organization
• Oncology experience.
• Demonstrated ability to lead or make major contributions to department, organizational and/or industry-wide initiatives, through effective communication and influence.
• Capable of applying innovative statistical thinking.
• Excellent interpersonal and communication skills.
• Capability in building and maintaining strong working relationships in a team setting.
• Strong influencing skills applied effectively across functions and levels of an organization
• Experience of working with and coordinating the work of CROs.
• Experience working with a Medical Affairs Organization is desirable.

Why GSK?

We're combining the power of genetic and genomic insights into what causes disease, with the speed and scale of artificial intelligence and machine learning (AI/ML) to make better predictions about who a treatment might work for, and why. We believe this powerful combination of data and technology holds the key to fundamentally transforming medical discovery for the better, improving R&D success rates and shaping how even the most challenging diseases, like neurological conditions and cancer, can be both prevented and treated. In 2021 we delivered four major product approvals: Cabenuva for HIV, Jemperli for endometrial cancer, Xevudy for COVID-19 and Apretude, our new long-acting medicine for HIV prevention.

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