Remote Regulatory Affairs Manager – European CTAs

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

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.