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You will be updated with latest job alerts via emailWe 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 practises; our Performance with Choice programme offers a hybrid working model empowering you to find the optimal balance between remote and inoffice work.
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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 nonregistrational 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 RealWorld Evidence (RWE) and Health Outcomes Research groups to manage a diverse portfolio of projects that support market access for GSK oncology products and latestage pipeline assets.
Join our team of industryleading experts in data analysis and methodological research. Our endtoend project support model offers statisticians the opportunity to collaborate throughout the drug development process from early clinical trials to product registration and ongoing market support.
In this role you will
Provide statistical expertise for nonregistrational 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 GSKsponsored 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 realworld 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 crossfunctional 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.
Why you
Basic Qualifications & Skills:
We are looking for professionals with these required skills to achieve our goals:
MSc or equivalent degree in a Statistical discipline
Relevant experiencefrom 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:
Please note the following skills are not necessary just preferred if you do not have them please still apply:
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 industrywide initiatives through effective communication and influence.
Excellent interpersonal and communication skills. Capability in building and maintaining strong working relationshipsin a team setting.
Experience of working with and coordinating the work of
Closing Date for Applications Friday 23rd of May(COB)
Please take a copy of the Job Description as this will not be available post closure of the advert.
When applying for this role please use the cover letter of the online application or your CV to describe how you meet the competencies for this role as outlined in the job requirements above. The information that you have provided
Why GSK
Uniting science technology and talent to get ahead of disease together.
GSK is a global biopharma company with a special purpose to unite science technology and talent to get ahead of disease together so we can positively impact the health of billions of people and deliver stronger more sustainable shareholder returns as an organisation where people can thrive. We prevent and treat disease with vaccines specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies investing in four core therapeutic areas (infectious diseases HIV respiratory/ immunology and oncology).
Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders its also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired encouraged and challenged to be the best they can be. A place where they can be themselves feeling welcome valued and included. Where they can keep growing and look after their wellbeing. So if you share our ambition join us at this exciting moment in our journey to get Ahead Together.
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race color religion sex (including pregnancy gender identity and sexual orientation) parental status national origin age disability genetic information (including family medical history) military service or any basis prohibited under federal state or local law.
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Director
Full-Time