Regeneron UK Limited Posted October 9, 2026

Manager Clinical Supply Systems

Uxbridge1, United Kingdom Full time
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Regeneron UK Limited is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Clinical Supply Systems Manager to join our Clinical Supply Systems Group, supporting our clinical trials in a hybrid setting. In this role, you will support Interactive Response Technology (IRT) systems while collaborating with clinical trial management, data management, biostatistics and clinical supply leads. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Mulitiple locations are being considered for this role (Hybrid)

Discover your role:

Lead IRT study-team support from protocol-aligned requirements through conduct and closeout.

Oversee vendor functionality, processes and performance through routine issue-resolution and risk-management meetings.

Manage deployment timelines and application launches with internal teams and vendors.

Maintain requirements, user guides, training materials and communication plans.

Coordinate user acceptance testing.

Coordinate randomisation and kit-list uploads with Clinical Logistics and biostatistics.

Develop vendor-supported clinical-team and site training, presenting functionality and requirements at investigator meetings or clinical research associate training when required.

You bring a collaborative, solution-focused mindset.

This role requires:

Bachelor’s degree or eight years’ equivalent experience.

Four years’ biotechnology/pharmaceutical experience, including two directly with IRT systems.

Clinical-trial IRT development experience, protocol interpretation and IRT/programming terminology knowledge.

International Council for Harmonisation/Good Clinical Practice and regulatory guideline/directive knowledge.

Microsoft Office Suite competency.

Understanding of current and future business trends.

Leadership, negotiation, mentoring and coaching skills.

Multitasking, prioritisation, problem-solving, project management and organisational skills.

Written, verbal and small/large-group presentation skills.

Cross-functional/cross-cultural awareness and matrix-working ability.

Disease/therapeutic-area knowledge is a plus.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process.  If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Job details

Seniority
Manager
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Uxbridge1, United Kingdom
Employment type
Full time

How this role compares

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

We currently track 596 comparable Manager Manufacturing & CMC roles across 97 biopharma companies.

596Comparable roles tracked
547Currently active
97Companies hiring similar roles
40Countries represented

Salary context

179 of 596 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Warehouse Associate I (M-F 11am-7:30pm) · AbbVie $16/hr – $29/hr (≈ $33,280–$60,320/yr)
Highest disclosed · Associate Director / Director - Biologics Drug Product Development · AbbVie $160,500/yr – $305,000/yr
Peer group range $46,800 – $232,750 (median $165,150)

Where these roles are based

Top locations among the 596 comparable roles

United States334
India50
Ireland24
Japan23
Netherlands19
China17

+ 34 more countries

Seniority mix

596 of 596 peers have a known seniority level

Manager350
Associate142
Associate Director104

Therapeutic area mix

6 of 596 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease3
Vaccines & Infectious Disease2
Immunology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Ipsen Biopharm Ltd Wrexham, United Kingdom Manager
Same function Same seniority Same country
60%similar
CSL Behring UK Ltd Maidenhead, United Kingdom Manager
Same function Same seniority Same country
60%similar
BioNTech London, United Kingdom Manager
Same function Same seniority Same country
60%similar
AstraZeneca London, United Kingdom Manager
Same function Same seniority Same country
60%similar
GlaxoSmithKline Services Unlimited Uk, United Kingdom Manager
Same function Same seniority Same country
60%similar
UCB Slough, Berkshire, United Kingdom Manager
Same function Same seniority Same country

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.

Or follow a whole field: get every new Manufacturing & CMC job in the United Kingdom, and choose locations and companies.

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.

60%
Production Manager
Ipsen Biopharm Ltd · Wrexham, United Kingdom · Manager
Function Therapeutic area Seniority Country
60%
Supply Chain Manager
AstraZeneca · London, United Kingdom · Manager
Function Therapeutic area Seniority Country
60%
Program Manager - New Product Introduction & Commercial Readiness
Ipsen Biopharm Ltd · Wrexham, United Kingdom · Manager
Function Therapeutic area Seniority Country
50%
Associate Director, Global Regulatory Science, CMC
Moderna Biotech Manufacturing UK Ltd · London, United Kingdom · Associate Director
Function Therapeutic area Adjacent 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.