Clinical Product Manager in London

Are you looking to impact and be part of something special, such as shaping the future of healthcare? Do you have a strong background in clinical safety and regulatory compliance within HealthTech or healthcare? Are you passionate about ensuring that medical software is safe and effective for healthcare professionals and patients alike?

At Semble, we are on a mission to enable health professionals to amplify their impact. We improve the way healthcare is delivered to millions of people by providing doctors and their teams with powerful, innovative, intuitive, and secure software. Our cloud-based clinical system is already used by thousands of clinicians, making their lives easier and saving them money, while structuring their health data to help research.

We are a passionate and driven team, proud to unite under strong cultural drivers:

• Impact - We do work that matters.
• Collaboration – We are in it together.

This role can be mostly remote in the UK (with regular travel to our London office). We are unfortunately not able to consider candidates located outside these locations at this stage.

What you will be doing

We have established the foundations of clinical safety at Semble and we're now looking for someone to build on this groundwork, adding both strategic depth and operational excellence. This role combines two key facets: ensuring compliance with clinical safety regulations, and a product build component, acting as the product and engineering teams' clinical representative with the gravitas to engage with our delivery teams and advise on our product roadmap with clinical insight and expertise.

Reporting to the Chief Product Officer (CPO), you will embed "clinical safety by design" into our product development and release processes across four key areas:

• Act as the clinical product management voice across cross-functional teams
  • Leverage your clinical background and frontline experience to influence what we build and how we build it. Partner with Product Managers, Engineers, Compliance and Designers, you will help assess the clinical feasibility and desirability of proposed features, ensuring that what we deliver genuinely fits into clinical workflows, solves real problems for healthcare professionals, and improves patient outcomes.
  • You will bring the clinician's voice into discovery and prioritisation, challenging assumptions, validating concepts through clinical expertise, and helping the team distinguish between what's technically possible and what's truly valuable at the point of care. This means actively advising Product Managers during roadmap discussions, providing clinical context that sharpens their decision-making, and ensuring that Semble's product direction is grounded in clinical reality.
  • Design and deliver role-based clinical voice training (e.g., Product, Engineering, Implementation, Support) and ensure employee onboarding includes clinical safety fundamentals, reporting mechanisms, and expected ways of working.
  • Partner with Compliance to ensure alignment with UK and EU expectations for health software safety and quality and respond to safety-related customer and regulatory enquiries across the UK and France.
• Own and evolve clinical safety operational workflows
  • Lead the development and implementation of Semble's clinical safety strategy and governance to ensure our software meets relevant requirements (e.g. DCB0129) and supports safe use at scale.
  • Oversee the clinical risk management process, ensuring potential clinical safety issues are proactively identified, recorded, assessed, mitigated, and tracked through to resolution.
  • Lead the creation and maintenance of clinical safety documentation, including the Clinical Safety Case / Safety Case Reports, Hazard Logs, and supporting evidence required for compliance, assurance, and audit purposes.
  • Define and report clinical safety KPIs to leadership, highlighting trends, key risks, and mitigation progress.
• Partner with our external nominated CSO and clinical safety tooling
  • Act as the single point of contact (SPOC) for our external nominated CSO, coordinating clinical safety activity, evidence gathering, reviews, and follow-ups.
  • Operate a clinical safety sign-off and release governance process in partnership with our external nominated CSO, ensuring clinical safety considerations are appropriately assessed for changes, releases, deployments, and configuration updates.
  • Ensure release decisions (including go/no-go, conditions to proceed, and residual risk acceptance) are documented and communicated appropriately.
• Serve as an internal and external advocate for clinical voice
  • Engage Semble's community of clinicians (internal teams, clients, and advisors) to ensure clinical feedback is incorporated into clinical safety practices, workflow design, and decision-making.
  • Collaborate with external bodies as required and represent Semble in audits, assessments, and inspections related to clinical safety and regulatory compliance.
  • Depending on your experience, support commercial conversations with prospects to address clinical safety requirements and demonstrate Semble's commitment to patient safety.

What we are looking for

We are looking for a pragmatic and detail-oriented experienced clinical safety professional who can manage risk, ensure compliance, and provide clear guidance to internal teams on all matters related to clinical safety.

• Extensive experience and formal training in clinical safety, with a strong understanding of relevant regulations and standards (e.g., DCB0129, DCB0160).
• Experience in working with cross functional teams with at least 3 years’ experience in a cross-team role.
• Current professional registration (e.g., as a clinician, nurse...) with at least 5 years’ experience as a practicing clinician.
• Previous experience as a Clinical Safety Officer (CSO) or in a similar clinical safety leadership role in a HealthTech company.
• Demonstrated ability to manage clinical risk effectively, with proven experience conducting clinical safety assessments and audits.
• Experience using a clinical safety platform such as Assuric.
• Strong understanding of regulatory frameworks in the UK, EU, and ideally other international jurisdictions.
• Ability to create and manage clinical safety documentation, including Safety Case Reports and Hazard Logs.
• Excellent communication and leadership skills, with the ability to translate complex regulatory requirements into practical guidance for cross-functional teams.
• NHS Digital Clinical Safety Practitioner accreditation (nice-to-have, not mandatory).
• Proficiency in the French language (nice-to-have, not mandatory).

What you’ll get in return

The great feeling coming with knowing you do something that matters: shaping the future of healthcare!

£70,000-85,000 package (based on your experience and the value you can bring).

Autonomy and ownership – we’ll set the vision and share the context, then we trust you to run with things – that’s the reason we hire you!

36 days off: 25 holidays +