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This role exists to support Evaro's ability to launch and improve treatment pathways by providing clinical input within established frameworks. The Clinical Doctor works on consultation improvements, patient communications, and compliance support - executing against playbooks and templates designed by senior clinical leadership. They work within Evaro's treatment launch engine alongside the Clinical Innovations Manager (who coordinates delivery) and Clinical Product Specialist (who handles documentation), providing medical input that keeps launches moving. The role creates value by delivering consistent clinical execution, flagging issues early, and freeing senior clinicians to focus on pathway design and strategic decisions.
Job Responsibility:
Executes clinical improvements to existing pathways within established guidelines
Improve existing consultations using per-question drop-off data and prescriber feedback
Draft updates to question wording, flow, and sequencing for review and approval
Support new pathway launches by preparing clinical content, risk assessments, and prescriber guidance to templates provided
Flag issues, ambiguities, or risks in consultation design
Document changes and maintain version control of clinical pathway materials
Drafts and maintains patient-facing content
Draft FAN emails and aftercare content
Use AI tools to produce patient education materials, with outputs reviewed before publication
Flag potential MHRA Blue Guide compliance concerns in marketing content
Maintain content libraries and update materials when clinical guidance changes
Collect patient outcomes data using questionnaires and other research techniques
Maintain data quality and flag collection issues
Prepare basic data summaries for review by senior leadership
Track status of CQC-related actions and flag overdue items
Support prescribing team in audit preparation by gathering information and documentation
Escalate compliance concerns promptly
Requirements:
GMC-registered medical doctor, F3+ or equivalent post-foundation experience
Able to work within established clinical frameworks and follow documented processes
Strong written communication skills - can draft clear patient-facing content
Comfortable using AI tools with appropriate supervision
Willing to learn UK healthcare regulation (CQC, GPhC, MHRA) requirements
Reliable, organised, and responsive to feedback
Nice to have:
A&E or other high-pace clinical background
Experience with digital health or patient-facing health products
Familiarity with MHRA Blue Guide advertising regulations
Interest in health tech and non-traditional clinical settings
What we offer:
Annual Leave: 25 days + Bank Holidays + birthday off