Senior Medical Lead

A Bit About Us

We’re Doccla , and we’re redefining where and how healthcare is delivered.

Our Virtual Ward and Remote Monitoring Solutions enable hospitals and health systems to care for patients at home. We support patients across the full care journey from early discharge and acute recovery to long-term condition management and proactive care.

We provide everything clinicians need to deliver safe, effective Virtual Care: medical-grade devices, logistics, patient onboarding, EHR integration, and an end-to-end clinical platform built around real-world workflows.

We currently work with over 60% of NHS ICBs and supporting health systems across the including UK, Ireland, France, and the DACH region to reduce hospital pressure, improve outcomes, and create a more resilient model of care.

We’re backed by top European investors, having secured £35m in Series B funding led by Lakestar, with participation from Elaia, General Catalyst, Speedinvest, and Bertelsmann.

Why Join Us?

This is your chance to join Doccla at a key stage in our growth .

We’re building the category leader in Virtual Care and Remote Patient Monitoring. You’ll be part of a highly entrepreneurial, mission-driven team that combines expertise across clinical, technical, commercial, and operational domains.

We’re solving real problems for patients and health systems and growing fast.

‍⚕️ What You’ll Do as a Senior Medical Lead

The Head of Clinical Innovation is a senior clinical leadership role responsible for translating Doccla's clinical model into safe, evidence-based, and commercially impactful products and pathways. The postholder provides the primary clinical interface between product development, regulatory compliance, and evidence generation ensuring that Doccla's technology and care model remain at the frontier of remote patient monitoring and proactive care.

This role sits within the CMO function and works in close partnership with the Chief Product Officer, commercial pathway leads, and external NHS partners.

✅ Key Responsibilities

CLINICAL PRO

• Lead the clinical input into product development priorities, including AI-enabled features, RPM device integration, and internal operational tooling.

• Provide overall clinical sign-off for new and updated product features, ensuring alignment with Doccla's clinical model and patient safety obligations.

• Lead DCB0129 / DCB0160 clinical safety compliance in partnership with the Clinical Safety Officer, including ongoing review and maintenance of the Hazard Log.

• Contribute to post-market surveillance activities, reviewing real-world clinical performance data and translating findings into product and pathway improvements.

• Chair or contribute to monthly cross-functional Clinical Safety Meetings, supporting preparation, facilitation, and governance administration.

• Clinical for implementation and associated pathway development

• Support delivery and implementation of virtual ward clients, ensuring pathways are evidence-based, operationally deliverable, and aligned to commissioner expectations.

• Support design and delivery of proactive care pathways, working with commercial and pathway leads to translate clinical evidence into scalable service models.

• Provide senior clinical input into commercial workshop programmes and bid development (SPRINT), particularly where pathway design or clinical credibility is central to the proposition.

• Clinical leadership for customer governance interface

EVIDENCE GENERATION & MDR COMPLIANCE

• Support Doccla's MDR evidence strategy, including the development of Clinical Evaluation Protocols (CEP) and Clinical Evaluation Reports (CER).

• Provide clinical sign-off for all MDR documentation, ensuring compliance with EU MDR Article 61 and associated MDCG guidance.

• Support NICE EVA (ARI) submission process for acute respiratory remote monitoring platforms.

• Lead state-of-the-art literature reviews and clinical evaluation activities in support of regulatory submissions, ongoing post-market clinical follow-up (PMCF), Doccla clinical interventions.

INCIDENT MANAGEMENT & CLINICAL RISK (PRODUCT-FOCUSED)

• Lead the organisation's clinical incident management process for product and device-related incidents, working with clinical, quality, and regulatory colleagues to triage, investigate, and close.

• Maintain oversight of product-related entries on the organisational Risk Register in partnership with the Clinical Governance Manager.

• Provide clinical leadership for MHRA device alerts and safety notifications relevant to Doccla's product portfolio.

What We’re Looking For

Essential

• Minimum 5 years certified General Practitioner (GP) in the UK, with active licence to practise

• Demonstrable experience in digital health, medtech, or NHS clinical informatics

• Working knowledge of MHRA / EU MDR, DCB0129/0160, and clinical safety frameworks

• Track record of contributing to clinical product development in a regulated environment

• Ability to synthesise clinical evidence and translate it into practical product and pathway decisions

• Comfortable operating at the interface of clinical, commercial, and technical functions

Desirable

• Experience of CER/CEP production or NICE submission processes

• Familiarity with remote patient monitoring, virtual wards, or proactive care models

• Experience working with NHS trust partners in a vendor or partnership capacity

• Postgraduate qualification in clinical leadership, health informatics, or medical education

How We Work

We empower everyone at Doccla to take ownership of their work and the company's mission. We act ethically and always put patient safety and outcomes first.

To thrive here, you’ll need a can-do attitude and an action-oriented approach , along with a willingness to learn and grow through open feedback.

We’re a hybrid team , with offices in London, Denmark, Germany . Most of our team is London-based and enjoys in-person time at our WeWork HQ 1–3 days per week, where you’ll find great lunch, barista coffee, and a pet-friendly space. Some of our teams are fully remote , depending on the team and responsibilities. This includes our Engineering, Clinical & Patient Support teams.

What You’ll Get

Annual Leave & Holidays
25 days annual leave + up to 8 UK bank holidays [this varies depending on the role]
Option to buy or sell holidays

Remote Working
Flexible remote options
Remote working stipend

Financial Benefits
Employee stock options
4% pension on full basic pay
️ 4x salary life insurance

Health & Wellness
Private health insurance
4 months full pay for birthing parent*
4 weeks full pay for non-birthing parent*
Phased return back to paid work
Sick pay

In-Office Perks (London HQ)
Free daily lunch
Pet-friendly office

Other Benefits
£500 L&D budget per person
Cycle to work scheme

Via Smart Health:
‍⚕️ 24/7 GP appointments
Mental health support
Nutrition & fitness advice
Second opinions & health checks

In Return for Your Hard Work

• A competitive compensation package (base + stock options), with half-year and annual performance reviews

• The chance to work on patient-first, system-level healthcare challenges in one of Europe’s leading healthtech companies

• Opportunities for growth and leadership we want you to challenge the status quo, own your impact, and continue developing, with our full support

Diversity at Doccla

We embrace diversity. To build a great product, we need a team with a wide range of perspectives, backgrounds, and experiences.

We’re committed to equal opportunity hiring regardless of race, religion, gender identity, sexual orientation, age, disability, or background. If you're excited about the role, we encourage you to apply even if your experience doesn't match every point.

Safer Recruitment

We are committed to safer recruitment practices. As Doccla is a CQC registered company, a Disclosure and Barring Service (DBS) check will be required for all roles.

It is an offence to apply for such work if you are barred from working with children or vulnerable adults.