Clinical Doctor Clinical · Norwich · Fully Remote
Cornerstone VC, Norwich, CT, United States
Clinical Doctor
About the Role
This is a hands‑on role with four core accountabilities:
Consultation Improvement & Support
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
Patient Communications & Content Support
Draft FAN (Further Answers Needed) 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
Research Data Collection Support
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
CQC Compliance Support
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
Decision Rights
To give you a clear picture of where this role sits:
You own (decide independently):
Minor wording and clarity improvements within approved consultation guardrails
Drafting content using established templates (subject to review)
Organising your own workload within agreed priorities
Flagging issues and concerns promptly
You recommend (propose, but someone else approves):
Consultation flow and sequencing change
Content updates and new patient communications
Process improvements to ways of working
You elevate (flag and hand‑up):
Any novel clinical judgement calls or situations not covered by existing playbooks
Patient safety concerns or potential incidents
Potential regulator compliance risks in content or advertising
Resource constraints or blockers affecting delivery
Anything requiring interpretation of clinical policy
Technical & Professional Competencies
Essential:
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
Preferred:
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
Location
This is a full‑time, remote (UK) permanent role with potentially 1‑2 days per quarter in our Norwich office.
Salary & Benefits
Salary:
£65000‑ £90000 DOE
Annual Leave:
25 days + Bank Holidays + birthday off
Health Plan:
Enhanced healthcare coverage
Leave:
Competitive parental, fertility, compassionate + bereavement leave policies
Growth:
Clear progression pathways and development opportunities
Culture:
Supportive, collaborative environment with structured onboarding
#J-18808-Ljbffr
About the Role
This is a hands‑on role with four core accountabilities:
Consultation Improvement & Support
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
Patient Communications & Content Support
Draft FAN (Further Answers Needed) 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
Research Data Collection Support
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
CQC Compliance Support
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
Decision Rights
To give you a clear picture of where this role sits:
You own (decide independently):
Minor wording and clarity improvements within approved consultation guardrails
Drafting content using established templates (subject to review)
Organising your own workload within agreed priorities
Flagging issues and concerns promptly
You recommend (propose, but someone else approves):
Consultation flow and sequencing change
Content updates and new patient communications
Process improvements to ways of working
You elevate (flag and hand‑up):
Any novel clinical judgement calls or situations not covered by existing playbooks
Patient safety concerns or potential incidents
Potential regulator compliance risks in content or advertising
Resource constraints or blockers affecting delivery
Anything requiring interpretation of clinical policy
Technical & Professional Competencies
Essential:
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
Preferred:
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
Location
This is a full‑time, remote (UK) permanent role with potentially 1‑2 days per quarter in our Norwich office.
Salary & Benefits
Salary:
£65000‑ £90000 DOE
Annual Leave:
25 days + Bank Holidays + birthday off
Health Plan:
Enhanced healthcare coverage
Leave:
Competitive parental, fertility, compassionate + bereavement leave policies
Growth:
Clear progression pathways and development opportunities
Culture:
Supportive, collaborative environment with structured onboarding
#J-18808-Ljbffr