Regulatory Affairs Manager

SEC Life Sciences; British Columbia; Remote; CAD 90,000 - 120,000; Part time

Job summary

A leading life sciences consultancy is seeking a Regulatory Affairs Manager for a remote contract role. Candidates should have over 8 years of regulatory experience and a strong background in technical writing. The manager will lead regulatory projects, author documentation, and mentor junior consultants. This contract offers significant autonomy while engaging with clients and overseeing project deliverables.

Qualifications

• 8+ years' regulatory experience in the life sciences sector.
• Hands-on expertise in managing marketing authorisation transfers (MATs).
• Strong knowledge of R&D processes and compliance standards.

Responsibilities

• Lead regulatory projects end-to-end, serving as the central point of contact.
• Independently author complex regulatory documentation.
• Oversee timelines and budgets, ensuring scope is tracked.

Skills

Regulatory expertise

Technical writing

Client interaction

Project management

Communication skills

Education

Degree in Life Sciences (BSc or MSc)

Job description

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Regulatory Affairs Manager (Contract) - UK Based

A unique opportunity has arisen for an experienced Regulatory Affairs professional to support a leading life sciences consultancy on a contract basis. Operating at the intersection of science and strategy, this organisation partners with a global client base across pharmaceutical, biotech, and medical device sectors to deliver critical regulatory solutions.

With a project pipeline spanning multiple complex submissions, this is an ideal role for a senior regulatory contractor who enjoys autonomy, technical writing, and shaping client outcomes across the full lifecycle of regulatory projects. This role is remote-based within the UK, with occasional client meetings as needed.

Your role as Regulatory Affairs Manager

Lead regulatory projects end-to-end, serving as the central point of contact and driving deliverables to completion.

Independently author complex regulatory and technical documentation with minimal oversight.

Act as a trusted advisor in client interactions, including direct meetings, progress reviews, and bid defence sessions.

Oversee timelines and budgets, ensuring scope is tracked and additional work is appropriately captured.

Mentor and review work from junior consultants, offering structured feedback and development support.

Contribute to internal process improvements, SOP reviews, and broader regulatory or cross-functional initiatives.

Experience and qualifications for the Regulatory Affairs Manager role

A degree in Life Sciences (BSc or MSc minimum) with 8+ years' regulatory experience in the life sciences sector.

Deep understanding of regulatory frameworks, with hands-on expertise in managing marketing authorisation transfers (MATs).

Confident in submission strategy and publishing tools, with strong knowledge of R&D processes and compliance standards.

Familiarity with pharmacovigilance requirements as they relate to MATs and regulatory documentation.

Proven ability to manage multiple high-priority projects while working independently and effectively.

Excellent communication and client-facing skills, with experience influencing internal and external stakeholders.

To apply for immediate consideration, please submit your CV or get in touch directly to learn more about similar contract opportunities in the regulatory affairs space.

Telephone Number This is a required field

Email Address This is a required field A valid email address is required.

CV, LinkedIn or Dropbox URL This is a required field

CV Upload Choose File This is a required field

LinkedIn / Dropbox URL This is a required field A valid LinkedIn URL is required, please ensure it begins with https://www.linkedin.com/ A valid DropBox URL is required, please ensure it begins with https://www.dropbox.com/

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