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.Scientist, Patient-Centered Outcomes Research(m/w/x)
Designing and deploying patient-centered outcome measures for drug development. Familiarity with psychometric validation or eCOA systems required. Focus on quantitative drug development strategies and patient voice capture.
Requirements
- Master’s or PhD in Psychology, Public Health, Biomedical Sciences, or related field
- Minimum 2-4 years supporting outcomes research, clinical trials, or digital endpoint development, or 0-2 years with advanced degree, ideally in pharma/biotech
- Familiarity with psychometric validation, eCOA system implementation, or data-driven design of COA instruments
- Growing understanding of drug development lifecycle and regulatory science, particularly for PCOR and digital endpoints
- Strong collaboration skills and proven cross-functional teamwork
- Ability to independently contribute to study documents and evidence packages, with sound decision-making and problem-solving
- Excellent strategic agility, critical thinking, and global mindset with respect for cultural differences
Tasks
- Lead design, validation, and deployment of patient-centered outcome measures
- Contribute to quantitative drug development strategies
- Ensure robust capture of patient voice and experience
- Guide measurement strategies for specific molecules or studies
- Develop and refine fit-for-purpose PCOM strategies
- Execute detailed research plans and validation studies
- Prepare health authority documentation and regulatory packages
- Support continuous improvement of PCOR methodologies
- Explore innovative tools and technologies for insight generation
- Build expertise in novel data types and advanced analytics
- Participate in industry consortia and scientific advancement
Work Experience
- 2 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
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.Scientist, Patient-Centered Outcomes Research(m/w/x)
Designing and deploying patient-centered outcome measures for drug development. Familiarity with psychometric validation or eCOA systems required. Focus on quantitative drug development strategies and patient voice capture.
Requirements
- Master’s or PhD in Psychology, Public Health, Biomedical Sciences, or related field
- Minimum 2-4 years supporting outcomes research, clinical trials, or digital endpoint development, or 0-2 years with advanced degree, ideally in pharma/biotech
- Familiarity with psychometric validation, eCOA system implementation, or data-driven design of COA instruments
- Growing understanding of drug development lifecycle and regulatory science, particularly for PCOR and digital endpoints
- Strong collaboration skills and proven cross-functional teamwork
- Ability to independently contribute to study documents and evidence packages, with sound decision-making and problem-solving
- Excellent strategic agility, critical thinking, and global mindset with respect for cultural differences
Tasks
- Lead design, validation, and deployment of patient-centered outcome measures
- Contribute to quantitative drug development strategies
- Ensure robust capture of patient voice and experience
- Guide measurement strategies for specific molecules or studies
- Develop and refine fit-for-purpose PCOM strategies
- Execute detailed research plans and validation studies
- Prepare health authority documentation and regulatory packages
- Support continuous improvement of PCOR methodologies
- Explore innovative tools and technologies for insight generation
- Build expertise in novel data types and advanced analytics
- Participate in industry consortia and scientific advancement
Work Experience
- 2 - 4 years
Education
- Master's degree
Languages
- English – Business Fluent
About the Company
F. Hoffmann-La Roche AG
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein führender Anbieter von pharmazeutischen Wirkstoffen und setzt sich für die Gesundheitsversorgung weltweit ein.
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