Roche Posted September 10, 2026

Product Manager - Clinical Study Design - RDT Biometrics and Clinical Evidence

Welwyn, Hertfordshire, United Kingdom FULL_TIME
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Roche 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

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

Product Manager - Clinical Study Design  - RDT Biometrics and Clinical Evidence 

Roche Digital Technology (RDT) is where innovation meets purpose. As a global team at the heart of Roche, we are a community of business-minded technologists committed to help shape tomorrow’s digital future of healthcare. Our mission is to power Roche through cutting-edge digital technologies, harnessing the potential of artificial intelligence, data, and scalable tech innovations. Driven by purpose and passion, we’re building a future where digital is a core strength across all of Roche, enabling smarter ways of working, unlocking human potential, and driving breakthroughs that truly matter for millions of patients around the world.

At Roche, we offer a hybrid work model that combines flexibility with in-person collaboration. For now, we require our employees to be in our offices on average two days per week. The specific office days may vary depending on business needs, such as workshops, conferences, town halls, team meetings, and other collaborative events.

The Product Manager – Clinical Study Design sits at the intersection of clinical science, product innovation, and technology delivery, helping shape the Study Designer , a digital product transforming how clinical trials are designed. This role combines strong product thinking, user and workflow understanding, and technical curiosity to translate complex clinical needs into intuitive, high-value digital capabilities. The ideal candidate is curious, collaborative, AI-minded, and passionate about using technology to enable smarter, faster, and more effective clinical study design.

The Opportunity

Understand Users & Workflows: Work directly with Clinical Scientists, Biostatisticians, Medical Writers, and other study team members to understand how clinical studies are designed today, where users struggle, and where technology can meaningfully improve their experience.

Shape Product Features: Partner with Product Managers, UX designers, engineers, and scientific experts to turn user problems and opportunities into product concepts, workflows, features, and incremental releases.

Drive Product Discovery: Participate in user interviews, discovery workshops, design sessions, prototyping, and experimentation to understand the problem before jumping to a solution.

Translate Problems into Buildable Products: Break complex clinical workflows into clear product capabilities, user journeys, stories, and acceptance criteria that engineering teams can act upon, while maintaining focus on the underlying user problem and intended outcome.

Prioritize for Value: Help evaluate competing requests and opportunities based on user value, business impact, technical complexity, dependencies, and product strategy rather than treating every request as a requirement.

Partner with Engineering: Work closely with engineers and architects throughout development, understanding technical constraints and tradeoffs and helping the team find pragmatic solutions without losing sight of the user experience.

Who You Are

Professional Experience: Requires significant years of experience in product management, senior business analysis, or hybrid product leadership with complex digital products, plus multiple years of hands-on experience in clinical trial design, clinical development, or closely related life sciences.

Education & Certifications: A Bachelor's degree in Life Sciences, Pharmacy, Biomedical Sciences, Computer Science, or Information Systems is required; a Master's degree or PhD in a clinical/scientific/biomedical field is preferred, and Business Analysis certifications (are highly valued.

Product Lifecycle & Requirements Management: Proven track record of managing the end-to-end product lifecycle from early discovery to live deployment and value measurement, backed by expert-level skill in writing structured user stories, acceptance criteria, functional specs, and traceability matrices. Demonstrated experience understanding user problems and translating them into workflows, product capabilities, user stories, prototypes, or software features.

AI and Technical Literacy: Curiosity about AI-enabled and data-driven products and demonstrated use of AI tools in day-to-day work. Preferred understanding of core software development concepts, including APIs, data models, microservices architecture, and cloud-based platforms like AWS, Azure, or GCP.

Agile Frameworks & Tool Proficiency: Offers extensive experience operating within agile/scrum frameworks, featuring hands-on ownership of backlog management and sprint execution while being highly proficient in tools like JIRA, Confluence, and Productboard.

Scientific Fluency & Systems Thinking: Possesses the scientific fluency to engage in deep, credible protocol design and regulatory conversations with physicians and researchers, combined with systems thinking to see how individual features connect to broader clinical workflows and patient outcomes.

Leadership, Influence & Adaptability: Proven ability to lead, build coalitions, and influence senior cross-functional stakeholders without formal authority; thrives with an innovation-oriented mindset and exhibits comfort with ambiguity when priorities shift or problems are undefined.

We look forward to your application !

#RDT2026

 

 

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

The statements herein are intended to describe the general nature and level of work being performed by employees, and are not to be construed as an exhaustive list of responsibilities, duties, and skills required of personnel so classified. Furthermore, they do not establish a contract for employment and are subject to change at the discretion of Roche Products Ltd. At Roche Products we believe diversity drives innovation and we are committed to building a diverse and flexible working environment. All qualified applicants will receive consideration for employment without regard to race, religion or belief, sex, gender reassignment, sexual orientation, marriage and civil partnership, pregnancy and maternity, disability or age. We recognise the importance of flexible working and will review all applicants’ requests with care. At Roche difference is valued and we are proud to be an equal opportunity employer where you are encouraged to bring your whole self to work.

Job details

Seniority
Manager
Function
Information Technology
Therapeutic area
Not listed
Location
Welwyn, Hertfordshire, United Kingdom
Employment type
FULL_TIME

How this role compares

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

We currently track 265 comparable Manager Information Technology roles across 40 biopharma companies.

265Comparable roles tracked
244Currently active
40Companies hiring similar roles
21Countries represented

Salary context

45 of 265 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 · AI and Agentic Engineer Associate · Exelixis Inc $103,000/yr – $145,000/yr
Highest disclosed · Associate Director, Business Analysis · $224,640/yr – $256,600/yr
Peer group range $124,000 – $240,620 (median $183,750)

Where these roles are based

Top locations among the 265 comparable roles

India115
United States86
Spain14
Greece8
Japan6
China6

+ 15 more countries

Seniority mix

265 of 265 peers have a known seniority level

Manager163
Associate Director55
Associate47

Therapeutic area mix

0 of 265 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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
Gilead Sciences Europe Ltd. Uxbridge, United Kingdom Manager
Same function Same seniority Same country
60%similar
Gilead Sciences Europe Ltd. Uxbridge, United Kingdom Manager
Same function Same seniority Same country
50%similar
Gilead Sciences International, Ltd. Cambridge, United Kingdom Associate Director
Same function Adjacent seniority Same country
50%similar
Gilead Sciences Europe Ltd. Uxbridge, United Kingdom Associate Director
Same function Adjacent seniority Same country
45%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same seniority
45%similar
Gilead Sciences, Inc. Foster City, United States Manager
Same function Same seniority

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.

60%
Senior Manager, IT – Product Lead, Global Value & Access (International)
Gilead Sciences Europe Ltd. · Uxbridge, United Kingdom · Manager
Function Therapeutic area Seniority Country
50%
Assoc Director, IT
Gilead Sciences Europe Ltd. · Uxbridge, United Kingdom · Associate Director
Function Therapeutic area Adjacent seniority Country
45%
Sr. Manager, IT Business Analysis – Medical Affairs
Gilead Sciences, Inc. · Foster City, United States · Manager
Function Therapeutic area Seniority Country
45%
Manager - IT Applications Lab Systems
Regeneron Pharmaceuticals, Inc (USA) · Rensselaer, United States · Manager
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.