Evidence Generation Strategy Lead

5 days ago

Slough, Slough, United Kingdom UCB Full time

About the Role

We are seeking a highly skilled and experienced Evidence Generation Strategy Lead to join our Patient Value Neurology Group at UCB. As a key member of our team, you will be responsible for leading regional Europe Epilepsy and Rare Syndrome Real-World Evidence (RWE) studies and Evidence Generation initiatives.

Key Responsibilities

  • Provide expert input to evidence generation initiatives planned and managed by local cross-functional teams across EU, supporting Launch and Market Access activities.
  • Help shape the use and acceptance of RWE in the external environment, collaborating with relevant internal roles.
  • Prove subject matter expert input in Clinical Study Teams and RWE practice.
  • Membership in relevant regional and global teams, including leading on the EU Integrated Strategic Evidence Generation group.
  • Act as a primary contact person and owner for RWE EU ERSO studies for vendors and internal stakeholders, including budget allocation.
  • Design study concepts, translate them into study protocols, co-work with all internal cross-functional roles.
  • Guide Clinical Development decisions concerning the selection of appropriate clinical/patient-reported endpoints, target patient populations, and RWE tools.
  • Oversee and be accountable for the execution of the RWE studies and other EG projects, including interim and final results delivery, interpretation, and communication of outcomes for internal decision-making.
  • Develop and execute proper and timely dissemination of the evidence gained in peer-review journals and congresses, based on the Strategic Publication Plan and according to Patient Value Brand Plans.
  • Collaborate with local medical teams and RWE partners identifying potential countries and sites for participation in RWE studies, including alignment with Key Opinion Leaders and professional organizations, organization of Scientific Advisory Boards.

Requirements

  • Minimum of MSc education.
  • Significant experience in the pharmaceutical industry.
  • Experience in medical affairs/RWE and preferably some experience in R&D/clinical development and publications.
  • Comprehensive knowledge of legal & regulatory requirements in R&D, including post-marketing research, NIS, other RWE.
  • Excellent understanding of clinical practice and RWE generation methodology.
  • Ability to translate pharma trends and healthcare ecosystem trends into opportunities through RWE generation.
  • Leading & Influencing matrix organization for patient value & Impact.
  • Proven leadership ability of internal and external cross-functional teams.

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