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Role Overview:
- Serve as a subject matter expert in patient-reported outcomes, shaping evidence strategies across the development lifecycle.
- Translate patient-centered needs into study designs, endpoints, and scientific deliverables.
Collaboration:
- Partner with Clinical Development, Biostatistics, Regulatory Affairs, Medical Affairs, and Clinical Operations.
- Engage with external experts, patient stakeholders, and research partners.
Growth:
- Start as individual contributor with potential to lead a team as the organization expands.
- Contribute to regulatory submissions, publications, and capability-building initiatives.
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