Remote Regulatory Manager - UK (Global Submissions)

Precision for Medicine; United Kingdom; Remote; GBP 70,000 - 95,000; Full time

Job summary

Precision for Medicine is recruiting a Regulatory Manager / Senior Regulatory Manager to join our growing global team. You will provide regulatory strategy and development guidance for clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely, well-organised submissions.

The ideal candidate has 5+ years regulatory experience for a Manager level and 7+ years for Senior Regulatory Manager, with CRO/pharma experience and

Qualifications

• Bachelor's degree in a scientific or healthcare discipline is required or equivalent experience.
• 5 years regulatory experience for Manager level and 7 years for Senior Regulatory Manager.
• Experience in CRO or pharmaceutical industry with submission know-how (CTA/IND, amendments, scientific advice).
• Ability to lead cross-functional teams and coordinate submissions for regional/global programs.
• Willingness to travel domestically and internationally.

Responsibilities

• Provide regulatory strategy across the clinical development lifecycle.
• Coordinate and prepare regulatory submissions to regulatory authorities and ethics committees.
• Serve as Global Regulatory Affairs representative in project teams.
• Lead/regulate regulatory activities to meet submission targets and maintain trackers and intelligence tools.
• Mentor regulatory staff and contribute to corporate quality initiatives.

Skills

Regulatory strategy

Global regulatory affairs

Leadership & mentorship

Stakeholder communication

Travel readiness

Education

Bachelor's degree in science/healthcare

Tools

Regulatory intelligence tools

Job description

Precision for Medicine is recruiting a Regulatory Manager / Senior Regulatory Manager to join our growing global team. You will provide regulatory strategy and development guidance for clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures, ensuring timely, well-organised submissions.

The ideal candidate has 5+ years regulatory experience for a Manager level and 7+ years for Senior Regulatory Manager, with CRO/pharma experience and