UCB Posted September 10, 2026

Drug Safety & Benefit-Risk Scientist (UK)

Slough, Berkshire, United Kingdom OTHER
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UCB has closed or removed this posting -- see current similar openings below.

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About this opportunity

Make your mark for patients 

We are looking for a Drug Safety & Benefit-Risk Scientist who is analytical, collaborative and adaptable to join our Patient Safety team in Slough, UK.

 

About the role

You will contribute to the evaluation of medicine safety and benefit-risk profiles across development and post-approval activities. Depending on experience, you may lead complex assessments, mentor colleagues and provide scientific guidance across projects.

 

Who you'll work with

You will be working in a team that partners closely with medical, clinical development, regulatory and safety experts to support informed decisions throughout the medicine lifecycle.

 

What you'll do

Evaluate safety and benefit-risk data to support scientific and regulatory decision-making.

Prepare safety assessments, reports and benefit-risk documentation for development and marketed products.

Interpret clinical and safety data and communicate key findings to cross-functional stakeholders.

Support signal evaluation, risk management activities and safety monitoring strategies.

Contribute to inspection-ready documentation and continuous process improvement.

For more experienced hires: mentor colleagues and lead complex benefit-risk deliverables.

 

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

Advanced degree in life sciences, pharmacy, medicine or a related discipline.

Experience in drug safety, pharmacovigilance, benefit-risk assessment or clinical development.

Ability to interpret complex scientific data and communicate insights clearly.

Strong written communication skills and experience preparing scientific documents.

Collaborative approach and ability to work across global multidisciplinary teams.

Additional experience leading projects or mentoring colleagues is an advantage.

 

Gender Neutrality & Inclusion Review

The advert has been reviewed for gender neutrality, inclusive language, clarity, simplicity, tone, grammar and spelling. No gender-coded language requiring replacement was identified.

Internal applicants should be in their current job for at least 12 months, must meet performance standards and are not on formal corrective/disciplinary process (PIP), warning, final warning, or compliance warning letters within the last 12 months. Please inform your Manager or your Talent Partner before applying to any internal job opportunities.

At UCB, we’ve embraced a hybrid-first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description, this role is hybrid with 40% of your time spent in the office, irrespective of your current contractual agreement. Should your current working arrangements differ, please contact your Talent Partner to discuss, before submitting your application.

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 EMEA-Reasonable_Accommodation@ucb.com . Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.

 

Requisition ID: 94002

Recruiter: Roya Paganini

Hiring Manager: Jo Collier

Talent Partner: Cornelius Luedtke

Job Level: MM II

Please consult HRAnswers for more information on job levels.

Job details

Seniority
Not listed
Function
Pharmacovigilance
Therapeutic area
Not listed
Location
Slough, Berkshire, United Kingdom
Employment type
OTHER

How this role compares

Computed from every other active Pharmacovigilance role in our database, not just this employer's listings.

We currently track 129 comparable Pharmacovigilance roles across 42 biopharma companies.

129Comparable roles tracked
121Currently active
42Companies hiring similar roles
25Countries represented

Salary context

36 of 129 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Technical Assistant, PV Operations · Mylan Pharmaceuticals Inc. $37,000/yr – $73,000/yr
Peer group range $55,000 – $429,500 (median $238,000)

Where these roles are based

Top locations among the 129 comparable roles

United States55
India9
France9
Japan8
Poland6
Germany6

+ 19 more countries

Seniority mix

85 of 129 peers have a known seniority level

Manager30
Director20
Senior18
Associate Director9
Associate3
Senior Director2
Principal2
Intern/Fellow/Postdoc1

Therapeutic area mix

15 of 129 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology9
Neuroscience3
Rare Disease2
Immunology1

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Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
PV Scientist Quality Document Manager
Biogen · Maidenhead, United Kingdom · Manager
Function Therapeutic area Seniority Country
25%
Associate Director - Pharmacovigilance (PV) Systems Strategy and Implementation
Lilly · Indianapolis, Indiana, United States of America · Associate Director
Function Therapeutic area Seniority Country
25%
Global Head of Patient Safety Operations
Roche · Basel, Basel-City, Switzerland · Seniority not listed
Function Therapeutic area Seniority Country
25%
Director, Patient Safety (MD)
Gilead Sciences, Inc. · Foster City, United States · Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.