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.
This is an exciting time to join us and help shape the future. It’s an opportunity to be part of something special.
Job Purpose:
The Associate Director, RWE will play a pivotal role in designing, implementing, and overseeing RWE strategies and initiatives to support our evidence generation activities. This person will be responsible for generating and leveraging real-world data to inform clinical trial design, generate evidence, and enhance decision-making throughout the drug development process and product claims processes.
Key responsibilities:
* RWE Strategy Development: Develop and implement a RWE strategy aligned with the business goals, ensuring that RWE is integrated into clinical development planning and decision-making.
* Internal capability building: Maintains a strong working understanding of clinical and epidemiological practice guidelines, clinical research models, protocol designs, real-world research development trends, and regulatory expectations. Guide the development of and deliver trainings for Haleon to enhance their knowledge and capability of RWE.
* Data Sourcing: Identify and collaborate with external data sources, such as electronic health records (EHRs), claims databases, and patient registries, to acquire relevant real-world data.
* Study Design: Provide specialist RWE input to the design of clinical trials by providing insights into patient populations, outcome measures, and endpoints based on real-world evidence.
* Data Analysis: Input to the analysis of real-world data to support clinical trial planning, participant recruitment, and endpoint validation.
* Evidence Generation: Generate high-quality real-world evidence that can be used to support regulatory submissions, reimbursement strategies, and market penetration initiatives.
* Cross-Functional Collaboration: Collaborate with cross-functional teams, including Safety, Regulatory Affairs, Categories and Business Units to ensure RWE strategy is aligned and is integrated into all phases of product development.
* Regulatory Compliance: Stay up-to-date with regulatory requirements related to RWE and ensure that all activities are compliant with relevant guidelines and regulations.
* Communication: Effectively communicate RWE findings and insights to internal and external stakeholders, including regulatory agencies, payers, and healthcare providers.
Knowledge/ Education / Previous Experience Required:
* Ph.D. or Master's degree in a relevant field (e.g., Epidemiology, Health Outcomes Research, Biostatistics).
* Extensive experience 7-10 years in real-world evidence generation within the consumer health, pharmaceutical or biotechnology industry.
* Strong knowledge of study design and drug development processes.
* Excellent communication skills and the ability to translate complex data into actionable insights.
* Leadership and project management experience.
* Regulatory knowledge related to RWE is essential.
Diversity, Equity and Inclusion
At Haleon 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.
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.
Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.
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