Regulatory Affairs Manager

RBW Consulting; Remote; GBP 60,000 - 80,000; Full time

Job summary

A consulting firm in the pharmaceutical industry is seeking a Regulatory Affairs Manager for an 8+ month fixed-term contract, fully remote. The role involves leading the preparation and submission of Clinical Trial Applications across Europe and requires significant experience in regulatory affairs within clinical trials. Candidates must have a Bachelor's degree, preferably in a life science discipline, and be based in either the UK or Sweden. This position offers flexible working and an opportunity to contribute to meaningful clinical projects.

Benefits

Flexible, remote working environment

Competitive FTC package

Collaborative team culture

Qualifications

• 4+ years' experience in a regulatory role within clinical trials.
• 5+ years' experience in submitting European Clinical Trial Applications.
• Strong hands-on experience with CTIS and IRAS.

Responsibilities

• Lead and support Clinical Trial Applications across Europe.
• Ensure timely and compliant submissions with internal and external teams.
• Collaborate with regulatory bodies for successful submissions.

Skills

Clinical Trial Applications (CTAs)

Regulatory submission planning

Experience with CTIS and IRAS

Collaboration with CROs

Education

Bachelor's degree in life science or equivalent

Job description

Regulatory Affairs Manager

8+ Month FTC | Fully Remote (UK or Sweden)

Are you an experienced Regulatory Affairs professional looking for your next impactful contract role? We are seeking a Regulatory Affairs Manager to support a growing portfolio of clinical development activities. This is an excellent opportunity to join a forward‑thinking team, work fully remotely, and play a key role in shaping regulatory strategies across Europe.

About the Role

As the Regulatory Affairs Manager, you will lead and support the planning, preparation, and submission of Clinical Trial Applications (CTAs) across Europe. You will collaborate closely with internal teams, CRO partners, and regulatory bodies to ensure timely and compliant submissions, while bringing your expertise to a portfolio of innovative clinical programs.

This is an 8‑month+ fixed‑term contract, with strong potential for extension.

Education Requirements

Bachelor's degree required, preferably in a life science discipline or equivalent.

What We're Looking For

• 4+ years' experience working in a regulatory role within clinical trials in the pharmaceutical or CRO industry.
• 5+ years' experience strategically planning, compiling, and submitting European Clinical Trial Applications.
• Strong, hands‑on experience with CTIS and IRAS, including full CTA preparation and submission.
• Previous experience working within a CRO environment is highly desirable.
• Exposure to national regulatory submissions, such as GMO and radiation safety applications, is preferred.
• Experience preparing County-specific ICFs is also beneficial.

Location & Working Model

• Fully remote role
• Candidates must be based in either the UK or Sweden
• Occasional travel may be required (minimal)

Why Join?

• Opportunity to support meaningful clinical development projects
• Work with a collaborative, dynamic team
• Flexible, remote working environment
• Competitive FTC package and immediate start availability