About the job
This role presents a unique opportunity for professional growth and leadership in advancing key clinical initiatives. Your responsibilities will encompass the following:
- Facilitate alignment of translational and clinical strategies with overarching project goals to ensure high-quality execution of Integrated Evidence Plans (IEP) and Clinical Development Plans (CDP).
- Generate essential clinical data to evaluate the efficacy, safety, and unique value propositions of investigational medicines, ensuring a swift path to patient benefit.
- Establish and oversee clinical milestones, timelines, and endpoints, including pharmacological and clinical efficacy criteria, to inform critical decision-making and Go/No-Go assessments for the CDP.
- Build and maintain collaborative relationships with cross-disciplinary teams across Biology, Translational Science, Clinical Operations, Regulatory Affairs, and more.
- Contribute to the implementation of strategic initiatives aimed at enhancing Clinical Development processes.
Clinical Development Strategy; Study & Program Design:
- Provide comprehensive oversight of R&D evidence generation to safeguard patient safety and ensure study success.
- Engage in study team discussions regarding indication planning, integrating diverse inputs to deliver critical milestones including early Medicine Profiles and Candidate Selection.
- Design robust clinical development plans and study protocols incorporating feedback from stakeholders such as patients, regulators, and pharmacovigilance entities.

