Director, Patient-Focused Evidence Global (remote)

 

Work Your Magic with us!  

 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  

 

United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.

 

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. 

 

Your Role:

As a Director for Patient-Focused Evidence working at a global level, you will lead the development of evidence strategies to capture and integrate the patient's perspective and patient experience data into drug research and development programs to address evidentiary requirements of health authorities and other stakeholders, supporting the end goal of patient access for EMD Serono's products.

 

Key responsibilities: 

1. Lead the development of evidence-generation strategies for collecting and integrating patient experience data and patient perspectives in programs in close collaboration with key internal and external stakeholders.
2. Lead the development of clinical outcome assessment (COA) measurement strategies, including the development of conceptual models, the selection, development, and validation of COA measures and endpoints.
3. Contribute to program Integrated Evidence Plans (IEPs) and other key program deliverables by facilitating consideration and inclusion of key patient experience aspects and related evidence gaps.
4. Contribute to the design and implementation of clinical studies (COA aspects), including study design, protocol writing, endpoint definition, data analysis planning, study report development, and dissemination.
5. Contribute to patient engagement activities related to program strategy or clinical studies, including patient advisory boards, panels or councils.
6. Serve as subject matter expert in applying mixed-methods, qualitative, and quantitative research techniques to address key business and research questions related to patient's experience across all drug research, development, and commercialization lifecycle phases.
7. Ensure high impact for deliverables by understanding business priorities and focusing on customer needs within a matrix organizational structure.  
8. Build, maintain and strengthen internal and external expert networks to anticipate, understand and/or inform changing evidence requirements from key external healthcare decision-makers.
9. Present research findings at national and international congresses and publish articles in scientific journals.
10. Maintain awareness of relevant new scientific, methodological, and regulatory developments.
11. Manage project-related contracting, budgets, vendor/partner oversight and management.

 

Who you are:

Minimum Qualifications:

• Master's degree in socio-behavioral sciences or health outcomes measurement e.g., health outcomes research, psychology, behavioral sciences, ethnography, or psychometrics.
• At least five years of experience working in the patient-centered research field within the life science industry, research organizations, academia, or consulting.

• Deep understanding of current regulatory and relevant professional societies' guidance on Patient-Focused Drug Development and the integration of patient experience data in drug research, development and commercialization.
• Demonstrable experience in leading the development or validation of new COAs, including clinician-reported outcomes (ClinROs), patient-reported outcomes (PROs), observer-reported outcomes (ObsROs), performance outcomes (Perfos), and digital clinical measures.
• Demonstrable experience in leading the preparation of COA evidence dossiers for submission to health authorities to support drug development programs or COA measure qualification

 

Preferred Qualifications:

• Doctoral degree in socio-behavioral sciences or health outcomes measurement e.g., health outcomes research, psychology,