Moderna Biotech Manufacturing UK Ltd Posted July 9, 2026

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

Oxford, United Kingdom Full time
Clinical Development

Moderna Biotech Manufacturing UK Ltd 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

The role

Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.  Moderna is establishing a leading research, development, and manufacturing facility at Harwell to support onshore mRNA vaccine production for respiratory diseases in the UK.

This long-term investment will create skilled jobs and strengthen collaboration with academic, NHS, and government partners. We welcome experts ready to help expand access to life saving vaccines. In this role, you will be at the heart of Moderna’s Immunoassays group, supporting assay development and clinical testing across a diverse therapeutic portfolio.

You will generate high-quality bioanalytical data that directly informs clinical trials, ensuring precision, integrity, and scientific rigor at every step.

Working in a highly collaborative and fast-paced environment, you will contribute to advancing Moderna’s mRNA platform while gaining exposure to cutting-edge laboratory technologies and emerging digital and AI-enabled tools.

Here's What You’ll Do:

Under the guidance of the study lead, take responsibility for the quality and integrity of assigned immunoassay projects supporting clinical trials at Moderna

Execute experimental work for assay development, qualification, and validation, as well as testing clinical samples

Conduct assay sample analysis and deliver high-quality data within defined timelines

Prepare laboratory experiments, including media, chemicals, and reagents, ensuring accurate batch record maintenance

Maintain laboratory space and support equipment maintenance to ensure operational excellence

Be trained in and adhere to Moderna-specific procedures and standards

Collaborate effectively across multiple projects, acting as a strong communicator to coordinate competing priorities

Identify, troubleshoot, and resolve quality issues, escalating to study or scientific leads as needed

May author bioanalytical plans and reports, and draft or review standard operating procedures (SOPs)

Ensure strict compliance with safety and regulatory guidelines at all times

Maintain up-to-date training records and demonstrate continuous learning

Assume general laboratory responsibilities as assigned to support team objectives

Operate primarily within a laboratory environment (≥85% of time), with flexibility for occasional overtime or weekend shifts as required

The key Moderna Mindsets you’ll need to succeed in the role:

“We obsess over learning. We don’t have to be the smartest we have to learn the fastest.”

“We digitize everywhere possible using the power of code to maximize our impact on patients.”

Here’s What You’ll Need (Basic Qualifications)

BSC/MSc Degree in Biology, Biotechnology or Life sciences with experience in a lab environment.

Demonstrated level of independence and work ethics

Good written, presentation and interpersonal communication skills

Good computational skills, preferably experienced with Word, Excel, Power Point, GraphPad Prism

Preferable knowledge of working in a regulated environment (GCP, ISO standards)

Preferable experience with LIMS systems.

This position is site-based, requiring you to be at Moderna’s site full-time. This position is not eligible for remote work.

As part of Moderna’s commitment to workplace safety, this role may require an enhanced pre-employment check.

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work.   That’s why our benefits and well-being resources are designed to support you, at work, at home, and everywhere in between.

Competitive healthcare, plus voluntary benefit programs to support your unique needs

A holistic approach to well-being with access to fitness, mindfulness, and mental health support

Family building benefits, including fertility, adoption, and surrogacy support

Generous paid time off, including vacation, bank holidays, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown

Savings and investments to help you plan for the future

Location-specific perks and extras

The benefits offered may vary depending on the nature of your employment with Moderna and the country where you work.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is committed to equal opportunity in employment and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodation or adjustments to qualified job applicants with disabilities. Any applicant requiring an accommodation or adjustment in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations and Adjustments team at leavesandaccommodations@modernatx.com .

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Job details

Seniority
Not listed
Function
Clinical Development
Therapeutic area
Not listed
Location
Oxford, United Kingdom
Employment type
Full time

How this role compares

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

We currently track 958 comparable Clinical Development roles across 91 biopharma companies.

958Comparable roles tracked
886Currently active
91Companies hiring similar roles
39Countries represented

Salary context

345 of 958 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 · Patient Safety Epidemiology Associate Director · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $458,800 (median $222,900)

Where these roles are based

Top locations among the 958 comparable roles

United States493
India142
United Kingdom54
China38
Poland35
Japan23

+ 33 more countries

Seniority mix

765 of 958 peers have a known seniority level

Manager202
Director180
Senior114
Associate Director101
Associate58
Executive/VP40
Senior Director38
Principal29
Intern/Fellow/Postdoc3

Therapeutic area mix

204 of 958 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology92
Immunology39
Neuroscience26
Cardiovascular / CVRM15
Respiratory12
Ophthalmology8
Dermatology & Aesthetics5
Rare Disease3
Vaccines & Infectious Disease3
Gastroenterology1

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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%
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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.