Disclosure Lead (m/f/d) (UK)

UCB S.A.; Slough; On-site; GBP 40,000 - 55,000; Full time

Job summary

UCB S.A. is seeking a detail-oriented Disclosure Lead to manage the compliance and transparency of clinical trial data. The role involves working with various teams to ensure accurate registration and reporting, directly contributing to the company’s commitment to ethical research. This position is ideal for candidates with a scientific background and experience in clinical development or regulatory affairs.

Qualifications

• 1–2 years of relevant experience in clinical development or regulatory affairs preferred.
• Experience with TrialScope Disclose and ClinicalTrials.gov is a plus.
• Strong communication and interpersonal skills required.

Responsibilities

• Manage trial registrations and global registry reporting.
• Coordinate review of registry and results information.
• Maintain records and project tracking systems.

Skills

Project Planning

Organizational Skills

Communication

Interpersonal Skills

Education

Bachelor’s or Master’s degree in a scientific discipline

Tools

MS Office

Clinical Trial Systems

TrialScope Disclose

ClinicalTrials.gov

EudraCT

CTIS

Job description

Make your mark for patients

Disclosure Lead (m/f/d)

We are looking for a Disclosure Lead (m/f/d) who is detail-oriented, collaborative, and proactive to join us in our Global Clinical Sciences and Operations team, based in Slough, UK.

About the role

You will be at the crossroads of science and operations, managing the disclosure of clinical trial data to ensure compliance and transparency. Your work will directly support UCB’s commitment to ethical research and public trust.

Who you’ll work with

You’ll collaborate with multidisciplinary teams including Clinical Project Management, Statistics, Medical Writing, Regulatory Affairs, and Safety. You’ll also engage with external vendors and global registry authorities.

What you’ll do

• Manage trial registrations and results reporting on global registries
• Coordinate stakeholder review of registry and results information prior to public release
• Maintain accurate records and update project tracking systems
• Serve as point of contact with registry QA groups
• Support local registry teams and ensure data consistency
• Deliver internal training on disclosure processes

Interested? For this role we’re looking for the following education, experience and skills

• Bachelor’s or Master’s degree in a scientific discipline
• 1–2 years of relevant experience preferred (e.g. clinical development or regulatory affairs)
• Experience with TrialScope Disclose, ClinicalTrials.gov, EudraCT, and CTIS is a plus
• Strong project planning and organizational skills
• Excellent English communication and interpersonal skills
• Proficiency in MS Office and clinical trial systems

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 around 8,500 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.

UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [e-mail]. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.