Data Transparency Lead (m/f/d) (Clinical Trial) (UK)

at  UCB

MAKE YOUR MARK FOR PATIENTS

We are looking for a Data Transparency Lead (m/f/d) who is accountable, strategic, and collaborative to join our Global Medical Writing team, based in our office in Slough, UK.

ABOUT US

UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.

ABOUT THE ROLE

As the Data Transparency Lead (m/f/d), you will be responsible for overseeing the global delivery of data transparency activities in compliance with transparency requirements. This includes ensuring that all transparency processes — such as the preparation of plain language summaries, Policy 0070 submissions, Health Canada PRCI submissions, and data sharing operations — are aligned with UCB’s policies and regulatory requirements. You will drive the development of best practices and ensure transparency activities are carried out consistently, ethically, and in accordance with global standards.

WHAT YOU’LL DO

• Represent the organization as the data transparency and anonymization point of contact, providing input and guidance on best practices.
• Lead and/or support the preparation of data and documents for transparency, disclosure, and data sharing.
• Lead the development of new data anonymization techniques in collaboration with service providers.
• Oversee the anonymization and redaction service provider, ensuring compliance with performance metrics and regulations.
• Provide anonymized clinical study data to qualified recipients within approved platforms.
• Assist with results and registration process tasks as needed.
• Support the Disclosure, Quality Control, Medical Writing Teams as needed
• Perform other tasks as assigned.

INTERESTED? FOR THIS ROLE WE’RE LOOKING FOR THE FOLLOWING EDUCATION, EXPERIENCE, AND SKILLS:

• Bachelor’s degree in a relevant field required; a Master’s degree is preferred
• Proven experience in managing global data transparency and disclosure or similar roles
• In-depth knowledge of clinical study transparency and data anonymization regulations
• Knowledge of disclosure requirements including registry and results posting
• In-depth knowledge of clinical development and clinical trials
• Knowledge of clinical and regulatory documents and submissions
• Excellent organizational and project management skills
• Ability to collaborate with cross-functional teams and manage global partnerships
• Experience with an Electronic Content Management systemAre 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!
  If you are interested to learn more about R&D within UCB, please find more information here R&D at UCB.