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Director of Real-World Evidence and Oncology Strategy
2 months ago
We are seeking a highly skilled and experienced Director to lead our Real-World Evidence (RWE) initiatives in Oncology. As a seasoned industry professional, you will be responsible for designing and implementing RWE strategies to support product development and regulatory submissions.
Key Responsibilities- Lead RWE Planning and Execution: Develop and execute RWE plans and studies throughout all stages of product development, from pre-clinical to post-marketing phases with a focus on Oncology.
- Apply Innovative Methodologies: Utilize cutting-edge epidemiological designs and methodologies to generate robust real-world evidence supporting product development and regulatory submissions.
- Collaborate with Cross-Functional Teams: Work closely with cross-functional teams to ensure alignment of RWE initiatives with regulatory requirements and business objectives.
- Regulatory Liaison: Serve as a liaison between the R&D team and regulatory agencies, providing expertise and guidance on RWE-related matters.
- Stay Up-to-Date with Industry Trends: Stay abreast of industry trends, regulatory guidelines, and emerging methodologies in epidemiology and RWE to continuously enhance the company's capabilities.
- Minimum 6 Years of Experience: Minimum of 6 years of experience in RWE, with a focus on Oncology within the pharmaceutical industry.
- Expertise in RWE Strategies: Demonstrated expertise in designing and implementing RWE strategies for development programs, including the application of innovative designs and methodologies.
- Adaptability and Communication Skills: Ability to adapt quickly to the evolving landscape of RWE and epidemiological research, particularly in the context of a highly innovative product pipeline.
- Strong Communication and Interpersonal Skills: Strong communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and external stakeholders.