Associate Director, Biostatistical Programming - Weybridge, United Kingdom - Haleon
Description
Associate Director, Biostatistical Programming:
- Weybridge, United Kingdom
- Research and Development
Job Description:
Site Name:
Weybridge St Georges Avenue
-
Posted Date: Nov Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands - including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum - through a unique combination of deep human understanding and trusted science. What's more, we're achieving it in a company that we're in control of. In an environment that we're co-creating. And a culture that's uniquely ours. Care to join us. It isn't a question.
With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we're uniquely placed to do this and to grow a strong, successful business.
This position provides expert statistical programming input and project management for statistical programming activities in relation to clinical trials and statistical activities executed by Haleon in multiple categories.
- Accountable for delivery of statistical programming activities for the categories/studies of responsibility
- Provides statistical programming input from protocol development through to publication and submissions where appropriate, including defining Haleon or external standards to be applied by Third Party Vendors
- Provides programming support for activities outside of clinical studies, such as due diligence, reuse of clinical study data, and training
- Directly works with Haleon study teams to correctly understand the programming and analysis data requirements for clinical trials in their area of responsibility
- Provides Third Party oversight of strategic and tactical partners as related to their area of responsibility including input/review of study documentation and maintenance of study specific oversight plans
- Statistical programming oversight for regulatory submissions
- Delivers expert technical knowledge and leadership to the business for statistical programming activities, helping to ensure best practice and achievement of business objectives based on science and values, including leading or providing input in departmental initiatives
_ Why you?_
Basic Qualifications:
- BSc level degree
- 8+ years of experience as a clinical statistical programmer on multiple therapeutic areas and multiple projects
- 1+ years of experience working with third party vendors and providing oversight for statistical programming activities
- 8+ years of experience on submitting data to regulatory authorities
- 1+ years of experience working with SAS and CDISC programming
Preferred Qualifications:
- Masters level degree
- Knowledge of Industry standards such as ICH, CDISC, requirements of regulatory authorities
_ Why Consumer Healthcare?_
Right now, we're on an incredible journey as we prepare to become the first independent, 100% focused consumer healthcare company.
Better everyday health is about improving the health and wellness of the consumers that we touch every year - over a billion and a half of them - and it goes beyond products.
It's about truly helping people manage their health proactively in different ways as consumer needs evolve.
With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we're uniquely placed to do this and to grow a strong, successful business.
Diversity, Equity and Inclusion
In Consumer Healthcare we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone.
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