Patient Centered Outcome Research (PCOR) LeadMake your mark for patientsWe are looking for a Patient-Centered Outcomes Research Lead who is collaborative, insightful, and dedicated to join our PCOR team, Patient Communities, based in our Brussels office in Belgium, Monheim Germany, or Slough UK.About The RoleYou will be working in a team that is responsible for evaluation of patient needs and preferences in therapeutic areas of interest. You will contribute to demonstrating the benefits of innovative patient solutions and accelerating patient access through regulatory and value demonstration activities.Who You’ll Work WithYou will be working in a diverse, cross‑functional team that generate patient experience data and evidence which meets external evidentiary standards and can inform external healthcare decision making.What You’ll DoLead development and implementation of PCOR strategy on clinical outcome assessments (COAs) and patient preference (PP) research from early development through to full lifecycle management.Lead research supporting the selection, development, and validation of PROs/COAs.Lead Patient Preference research activities.Provide expert input to clinical development, regulatory and HTA briefing packages and submissions.Lead scientific dissemination of patient experience evidence in line with publication strategies.Build relationships and partner with external groups to advance methodological frameworks and acceptance of patient experience evidence to inform external healthcare decision making.Drive organizational awareness and education on patient‑centered outcomes and patient preference research.QualificationsAdvanced degree (Ph.D., M.D., Master’s, or equivalent) in a relevant field.Significant experience in PCOR within biopharmaceutical, medical device companies, or academia.Knowledge of clinical outcome assessment (COA) and patient preference (PP) research methodologies and evidentiary requirements by regulatory and HTA bodies.Strong project leadership, stakeholder management, and communication skills.Experience in clinical development process and appreciation of scientific content of clinical programs, e.g. trial design, protocol development, and statistical analysis.Ability to collaborate in a matrix environment and build internal and external partnerships.About UsUCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.Why work with usAt UCB, we don’t just complete tasks, we create value. We are collaborative, innovative, and patient‑focused. Our hybrid‑first approach fosters flexibility and teamwork.UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. #J-18808-Ljbffr