Clinical Safety Officer

🌍 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  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, Speed invest, and Bertelsmann.

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.

We are seeking a highly skilled and experienced Clinical Safety Officer to join our dynamic team.

The Clinical Safety Officer will play a pivotal role in our rapidly scaling health tech organisation, ensuring the safety and regulatory compliance of our cutting-edge health technology solutions. This role involves monitoring and evaluating the safety of our products, developing and implementing risk management plans, and ensuring adherence to regulatory requirements. The ideal candidate will possess a strong background in clinical safety, risk management, and regulatory affairs within the health tech industry.

They will collaborate with cross-functional teams to uphold the highest safety standards, ensuring our innovative solutions improve patient outcomes while adhering to regulatory requirements.

• Lead on clinical safety activities including compliance with NHS Digital DCB 0129/0160, UK MDR 2002 (SI 2002/618) and EU MDR 2017/745 under responsibility of the CMO/ DCMO.
• Develop, implement, and maintain clinical safety protocols and risk management plans according to ISO 13485 and ISO 14971.
• Monitor and evaluate the safety performance of health tech products throughout their lifecycle ISO 14971, ISO 13485, and DCB 0129/0160.
• Conduct safety assessments and risk analyses, ensuring compliance with relevant regulatory requirements.
• Lead Clinical Safety meetings and represent clinical safety at Clinical Governance Meetings.
• Leading Hazard Workshops using structured methods (e.g., HAZID, SWIFT) with multidisciplinary stakeholders such as developers, clinicians, and RAQA.
• Maintain and update Clinical Safety Case Reports and Hazard Logs in line with DCB 0129/0160, and manage the organisational incident log to support learning and continuous improvement.
• Stay current with clinical safety standards and regulatory guidelines relevant to health technology.

Regulatory Compliance:

• Ensure all clinical safety activities comply with relevant regulations, including DCB, UK/EU MDR, and other global standards.
• Prepare and maintain clinical evaluation reports (CERs) and other required documentation for regulatory submissions according to the most relevant guidelines.
• Assist in the preparation of technical files and regulatory submissions for market approval.
• Collaborate with regulatory affairs to address compliance-related issues or queries.

  Adverse Event Reporting:

  • Oversee the identification, documentation, and reporting of adverse events and incidents related to health tech products.
  • Conduct thorough investigations of safety-related incidents and develop corrective and preventive actions (CAPAs).
  • Ensure timely and accurate reporting of adverse events to regulatory authorities, including documentation through appropriate systems.

  Cross-Functional…