Manufacturing jobs in Grande-Bretagne

At Regeneron, we believe that when the right idea finds the right team, powerful change is possible. As we work across our growing global network to invent, develop, and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing, and commercialization. And new ways to think about health.

As a key member of Global Clinical Trial Services team, Regeneron is now looking for a Senior Manager, Digital Health Technologies, who will lead the implementation of digital tools & technologies in clinical research studies.

A great opportunity to join a passionate, dedicated & collaborative international team.

Office Based - Uxbridge

• Implement and coordinate digital tools and technologies (e.g., eCOA, eConsent, wearables, sensors, spirometry, ECG) in individual clinical research studies from study design to close-out.
• Manage project timelines, translations, specifications, and user acceptance testing (UAT) for supported technologies, ensuring compliance with Regeneron SOPs and ICH/GCP.
• Collaborate with study teams for both internally sourced studies and studies outsourced to CROs, balancing direct leadership and oversight.
• Build and enforce standards for tools & systems, lead vendor performance, and support training and education for stakeholders.
• Participate in process improvement initiatives in global development.
• Successfully implement digital tools and technologies across clinical trials, ensuring quality and compliance.
• Act as a patient technology expert, addressing raised issues.
• Responsible for the selection of the digital tool and technology vendor selection, in collaboration with study team
• Connect with stakeholders and escalate risks when vital.
• Provide input into protocol development regarding digital tools and technologies.
• Lead the creation of standards for digital tools and technology systems & coordinate vendor selection and performance.
• Run project plans, risk mitigation, documentation, and financial components
• Responsible for direct supervision of staff

• Strong knowledge of digital health technologies, particularly eCOA systems development processes.
• Demonstrated interpersonal and leadership skills, with an ability to independently balance multiple tasks and meet deadlines in complex environments.
• Effective communication skills, both verbal and written, with the ability to influence and work collaboratively.
• Technical proficiency in trial management systems and Microsoft Project Server.
• Knowledge of ICH/GCP and regulatory guidelines/directives.
• Project management skills, cross-functional team leadership, and organisational abilities.

To be considered for this opportunity you must have 8+ years of pharmaceutical digital health project management experience and hold a Bachelor’s degree.

Does this sound like you? Then connect with us, so we can learn more about you, and you can learn more about us. And join us, as we build a future we believe in.