Head of Regulatory Affairs

What you'll be doing:

• Lead Regulatory Strategy: Develop and spearhead the implementation of regulatory strategies that align with our long-term business objectives. Work closely with product development, customer success, and operations teams to ensure regulatory considerations are integrated from the ground up.

• Regulatory Consultancy to Business: Act as the primary regulatory advisor, providing expert guidance to internal teams on issues such as market entry, product compliance, and operational adjustments required by regulatory considerations.

• Conduct Audits: Oversee and conduct comprehensive audits, ensuring that all business practices not only comply with current regulatory standards but also uphold our commitment to operational integrity and excellence.

• Ensure Compliance: Monitor ongoing compliance with all relevant regulations, and lead efforts to adapt practices in response to evolving regulatory landscapes, particularly in key markets like the US and UK/EU.

• Influence External Regulatory Policies: Engage with industry groups and regulatory bodies to influence and shape external regulatory policies, positioning the company as a thought leader within the healthtech sector.

🫵 This job is for you if you:

• Possess extensive regulatory expertise, particularly in Good Clinical Practice, and have a strong understanding of the regulatory environments in the US and UK/EU.

• Have a background in life sciences, with a strong preference for experience in the healthtech industry.

• Are skilled in navigating complex regulatory frameworks and can effectively translate these challenges into actionable business strategies.

• Thrive in dynamic environments and approach problem-solving with agility and innovation.

• Demonstrate a digital mindset, being data-driven and customer-obsessed, to continuously improve our regulatory processes and customer interactions.

💫 Even better if you have:

• A track record of providing detailed regulatory guidance for study designs, protocol development, and informed consent processes, enhancing the quality and compliance of our projects.

• Experience leading and influencing regulatory discussions at a national or international level, contributing to broader industry standards and practices.

• Proven excellence in communication, capable of articulating complex regulatory issues in simple terms for diverse audiences, including regulatory bodies, internal teams, and industry groups.

🛑 Please note:

We can only accept applications from those eligible to live and work in the UK or in the USA (for specific roles). We are unable to sponsor visas for this position.

In addition, as part of our due diligence process, we will be conducting basic DBS checks on successful candidates. As per the The code of practice published under section 122 of the Police Act 1997, we are committed to treating all candidates fairly and are happy to share our Equal Opportunities and Ex-Offender policy on request.

Sano Genetics welcomes applications from all candidates irrespective of age, disability, gender, gender identity, sexual orientation, race, religion or belief, or marital or civil partnership status.

Team

Legal & Regulations

Role

Regulatory & Compliance

Locations

Remote UK

Remote status

Fully Remote

Yearly salary

£90,000 - £120,000

Employment type

Full-time

Perks & Benefits

• 🎒 Remote-First Workplace

• 🗺️ Up to 45 working days of remote work from anywhere in the world

• ⏱️ Flexible Working Hours

• 💻 Company Issued Laptop

• 🎉 Bi-Annual Offsite Socials

• 📈 EMI Stock Option Grants

• 🏡 £600 Work From Home Allowance

• 🧘 £600 Wellbeing Budget

• 👵👴🧓 Up to 5% Matched Pension Contribution

• 🚲 Cycle to Work and Tech Salary Sacrifice Scheme

• 🏝️ 25 Days as Standard + 8 Bank Holidays

• 🛩️ Up to 40 Days through buy-back

• 🔎 £1,000 p/y for Learning & Development

• 🥅 Full Health Insurance & Private Healthcare

• 🦷 Premium Dental Insurance

• 🏡 Life & Income Protection Insurance

• 🐣 Workplace Nursery Sacrifice Scheme

• 🍼 16 Week of full parental leave