We are seeking an experienced Senior HEOR Manager (m/w/d) to lead Clinical Outcome Assessment (COA) and Patient-Reported Outcome (PRO) strategies across multiple therapeutic areas for our custome rin Basel. This role will support clinical development programmes by generating high-quality patient-centred evidence for regulatory, HTA, and market access purposes.

Key Responsibilities

• Develop and execute COA/PRO strategies across clinical programmes.
• Advise study teams on the selection and implementation of COAs in clinical trials.
• Lead cross-functional COA projects with Clinical Development, Medical Affairs, Regulatory Affairs, Market Access, Biostatistics, and external vendors.
• Oversee COA validation activities, psychometric analyses, and interpretation of results.
• Support regulatory submissions, HTA dossiers, scientific publications, and conference presentations.
• Ensure compliance with FDA, EMA, and HTA requirements and industry best practices.
• Drive vendor management activities related to qualitative research, translations, and eCOA implementation.
• Stay current with developments in outcomes research and patient-centred evidence generation.

Required Qualifications

• Master's degree or PhD in Health Economics, Epidemiology, Psychology, Life Sciences, Pharmacy, Biostatistics, or a related field.
• Proven experience in HEOR, Outcomes Research, COA/PRO Strategy, or Patient-Centred Evidence Generation within the pharmaceutical industry.
• Strong knowledge of regulatory and HTA requirements.
• Experience working in global, cross-functional teams.
• Strong analytical, critical thinking, and problem solving skills, with ability to collaborate effectively in a matrix environment
• Excellent project management and stakeholder engagement skills.
• Languages: English. German is nice to have.

Contract Details

• Contract Type: Temporary (12 months)
• Start Date: December 2026
• Location: Basel, Switzerland
• Workload: 100%