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Clinical Program Delivery Lead


Raleigh, North Carolina, United States

Job Function:  Clinical Development
Job ID:  67908

Help us transform patients' lives.

At UCB, we put our heart, soul and skills into making a difference for people living with significant unmet needs. Working together, we blend the best of our talents to deliver thoughtful solutions that patients value. Will you join us in this pioneering adventure?





To strengthen our Global Clinical Sciences and Operations Team, based in our RTP office in Raleigh, NC, we are looking for a talented individual to fill the position of Clinical Program Delivery Lead


As a Clinical Program Delivery Lead you will:

  • Serve as point person within GCSO for program level operational updates and issues, ensuring open, transparent communication with GCSO team members, line management and GCSO strategic partnering liaisons
  • Provide operational expertise and support to the clinical development strategy of a UCB compound.  This would be for various indications, starting at the ‘First in Human’ stage (DP3) and continuing throughout the product lifecycle.
  • Drive scenario planning in the program by providing high level budget and timeline estimates
  • Liaise and engage with Key Opinion Leaders (KOL) to support the program
  • Contribute to the implementation of the Clinical Development Plan (CDP) through strategic oversight of operational activities managed by one or more clinical project managers (CPMs) ensuring project management consistency and alignment across studies and indications within a program.


You will contribute by:

  • Being responsible for the overall clinical operational leadership within GCSO, being the point of contact for the assigned program, Phase I - IV
  • Working closely with the Clinical Program Director (CPD) and CST Lead integrating scientific knowledge and operational excellence in collaboration with the CPM to ensure excellence in translation of CDPs into efficiently delivered studies
  • Driving feasibility and scenario planning for country considerations and risk/mitigation strategies for recruitment on a program level
  • Responsible for providing operational expertise in the clinical development of key program documents across the lifecycle of a program
  • Collaborating closely with Site Engagement, Patient Engagement and Strategic Feasibility as early as possible to project meaningful study recruitment rate estimates and timelines
  • Providing strategic oversight of operational activities managed by one or more CPMs within a clinical program and ensure there is consistency across the program.
  • Supporting Clinical Project Managers in ongoing study budget and timeline forecasting to ensure studies remain on time and in alignment with actual spend as well as trade-off analysis discussions, continual proactive assessment of risk identification/mitigation strategies


Interested? For this role we would prefer the following education, experience and skills:

  • Master’s degree of equivalent experience working in the SME space for 10 years that can be in lieu of an advanced degree
  • At least eight years of relevant experience in clinical trial management including team leadership
  • Experience managing several in-house and/or outsourced regional or global multi-center clinical studies from study start-up to study report completion
  • Substantial experience in study management and proven ability to manage complex, multinational studies
  • Possess strong technical background in biopharmaceutical research and a thorough understanding of good clinical practice and the clinical research development process
  • Strong team leadership skills
  • Effective stakeholder management skills
  • Ability to develop and manage study budgets
  • Ability to motivate, mentor, and lead individuals on multi-disciplinary international teams
  • Ability to manage multiple concurrent responsibilities in an environment of changing priorities
  • Strong negotiation skills
  • Strategic planning and execution ability at program level
  • Demonstrated ability to address/solve both simple and complex issues
  • Ability to develop and implement risk mitigation plans


Why you should apply

At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.


If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.



About Us

At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.

With a team of approximately 7,500 employees worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decisionmakers across the heath care ecosystem.

Curious to know more? Please visit our website www.ucb.com.


UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.

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