Healthtech Regulatory Counsel Needed Long-Term
Budget: $2 – $8 USD
Company
Fusatech is building a platform that must meet CBPM expectations, SaMD-style scrutiny and strict data protection standards. Our advisory board includes a Johns Hopkins professor and experienced UK medical directors, and we are designing for real-world clinic and pharmacy workflows.
Role
We need a freelance Legal & Regulatory Counsel with healthtech and/or CBPM experience to provide lean, pragmatic support across contracts, IP and regulatory responsibilities.
Key responsibilities
Review and update contracts and agreements (advisory board, pilot clinics, pharmacies, vendors, contractors).
Help design and maintain IP documentation: NDAs, IP assignment, licences and data-sharing terms.
Summarise key regulatory and compliance requirements that affect our product and pilot operations.
Track important legal and regulatory deadlines and flag actions to the team.
Review key patient, clinic and commercial documents for legal and regulatory risk.
Help Francesca create simple contract and compliance checklists that non-lawyers can follow.
Who you are
Hard-working and comfortable operating in a lean startup with limited support.
Highly responsive and able to work within 09:00–21:00 UK time, Monday–Saturday.
Take initiative in spotting legal and regulatory issues before they become blockers.
Think strategically about risk: focus on what matters most for this stage and product.
Logical and concise in how you explain legal concepts to non-lawyers.
Data-driven and evidence-orientated, comfortable grounding advice in guidelines and precedent.
Reporting to
Francesca, Business Manager.
Fusatech is building a platform that must meet CBPM expectations, SaMD-style scrutiny and strict data protection standards. Our advisory board includes a Johns Hopkins professor and experienced UK medical directors, and we are designing for real-world clinic and pharmacy workflows.
Role
We need a freelance Legal & Regulatory Counsel with healthtech and/or CBPM experience to provide lean, pragmatic support across contracts, IP and regulatory responsibilities.
Key responsibilities
Review and update contracts and agreements (advisory board, pilot clinics, pharmacies, vendors, contractors).
Help design and maintain IP documentation: NDAs, IP assignment, licences and data-sharing terms.
Summarise key regulatory and compliance requirements that affect our product and pilot operations.
Track important legal and regulatory deadlines and flag actions to the team.
Review key patient, clinic and commercial documents for legal and regulatory risk.
Help Francesca create simple contract and compliance checklists that non-lawyers can follow.
Who you are
Hard-working and comfortable operating in a lean startup with limited support.
Highly responsive and able to work within 09:00–21:00 UK time, Monday–Saturday.
Take initiative in spotting legal and regulatory issues before they become blockers.
Think strategically about risk: focus on what matters most for this stage and product.
Logical and concise in how you explain legal concepts to non-lawyers.
Data-driven and evidence-orientated, comfortable grounding advice in guidelines and precedent.
Reporting to
Francesca, Business Manager.