Pipeline Field Medical Lead

Make your mark for patients

We are looking for a scientifically credible, adaptable, and highly collaborative Pipeline Field Medical Lead to join our Medical Affairs and Clinical Development organization in the United States. This is a field-based individual-contributor opportunity supporting investigational programs and clinical research sites. The final territory, therapeutic-area assignment, and timing will be confirmed according to pipeline priorities and site activation.

You will serve as a field-based scientific partner to investigators, site staff, and scientific experts supporting enterprise-critical development programs. Working in a strictly scientific, non-promotional capacity, you will strengthen site engagement, support study startup and enrollment, and help resolve scientific or operational barriers. You will typically support two or more programs, with assignments evolving as the pipeline and site footprint change.

You will report to a Global Pipeline Medical Lead or Regional Field Medical Lead and partner closely with Clinical Operations, Clinical Development, clinical research associates, contract research organization teams, Medical Affairs colleagues, and other functions as appropriate. Externally, you will build compliant relationships with investigators, site staff, scientific experts, and research institutions while maintaining functional independence and scientific integrity.

• Lead scientific engagement with investigators, site staff, and scientific experts.
• Support site identification, selection, startup, enrollment, and study execution.
• Translate complex protocols into clear, scientifically rigorous site discussions.
• Identify barriers and coordinate solutions with clinical and cross-functional partners.
• Capture field insights and communicate them compliantly to internal study teams.
• Support multiple programs as therapeutic and geographic priorities evolve.

• Doctoral-level scientific or clinical degree, such as MD, PharmD, or PhD.
• 5+ years in field medical or clinical research roles.
• Experience as a medical science liaison, clinical research associate, or equivalent.
• Pharmaceutical or biotechnology clinical-development experience supporting scientific objectives.
• Strong scientific communication, presentation, relationship-building, and stakeholder-management skills.
• Ability to travel to sites, congresses, and regional meetings.

• Hands-on clinical-trial site startup or enrollment-support experience.
• Working knowledge of Good Clinical Practice and US clinical-research requirements.
• Experience in autoimmune disease, rheumatology, neurology, or relevant indications.
• Established relationships with investigators, healthcare professionals, or clinical research sites.
• Experience supporting two or more concurrent development programs.
• Success working independently in a changing, field-based pipeline environment.

• The reasonably anticipated salary range for this position is $182,000 - $239,000 per year. The actual salary offered will take into account related knowledge, skills, experience and location among other factors and may fall outside the expected range.

Are you ready to 'go beyond' to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!

About us
UCB 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 us?
At UCB, we don't just complete tasks, we create value. We aren't afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We 'go beyond' to create value for our patients, and always with a human focus, whether that's on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.

At UCB, we've embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless explicitly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable federal, state, or local law. UCB invites you to voluntarily self-identify during the application process. Provision of self-identification information is entirely voluntary and a decision to provide or not provide such information will not have any effect on your application for employment, your employment with UCB, or otherwise subject you to any adverse treatment. Any information you provide will be considered confidential and will be kept separate from your application and/or personnel file and will only be used in accordance with applicable laws, orders, and regulations.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on US-Reasonable_Accommodation@ucb.com for application to US based roles. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.