Freelance/Contract Regulatory Affairs Project manager

1 week ago

London, Greater London, United Kingdom ProPharma Group Full time £60,000 - £120,000 per year

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

ProPharma is continuing to be an integral partner of a global life-sciences brand as they require project support within their Regulatory Affairs group within the EU. This role in particular is to act as a Regulatory Affairs Project for their Clinical trial applications (CTA's) within the EU space with demonstrated experience in the area being a must. The project will commence in January 2026; it is a full-time position (1.0 FTE) and can be performed fully remotely throughout anyway within the UK or EU. It will run for at least 6 months initially but with a high chance of extending and we would prefer support from an independent consultant.  

Responsibilities included:

  • Provide guidance and support as a project leader on a cross functional basis within the Regulatory Affairs CTA group

  • Work effectively with various stakeholders to ensure each projects success

  • Lead the preparation, review and submit regulatory clinical trial applications within the EU

  • Ensure all submission activities meet key regulations within the region

  • Ensure compliance is achieved to the EU CTR regulations throughout each project

  • Implement and submit key documentation on to our clients systems

  • Provide key project leadership across a range of groups

  • Ensure all timelines and milestones are achieved throughout the project

  • Overall support our client with strategic and operational goals within the Regulatory Affairs CTA space

Skills required

  • Must be educated within a life science discipline to at least a BSc or higher

  • Proven experience working within Regulatory Affairs linked to Clinical trial applications is a must

  • Can demonstrate key project management skills within a similar setting

  • Thorough experience working to all key regulations within the EU

  • Strategic and operational skills within the area are a must

  • Fluency in English is a must

  • Can perform the project to the requirements set out within the job description

#LI-DNI

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.

All applications to roles at ProPharma are personally reviewed by a member of our recruitment team. We do not rely on AI screening tools to support our hiring process. You will always receive an outcome to your application so that you have an answer from us - whether you're successful or not.

***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

  • Freelance - Clinical Project Manager (0.8 FTE) (Remote)

    2 weeks ago

    London, Greater London, United Kingdom EPM Scientific Full time £60,000 - £80,000 per year

    EPM Scientific are currently partnered with a Biotechnology company who are seeking aFreelance Clinical Project Managerto support their upcoming Oncology Trials in the EU. See a short summary below:Contract Conditions:Start date: ASAPLocation: European Union (Remote)Contract: FTE, 12-Month ContractProject: Oncology - Phase 3 Global TrialKey...

  • Senior Manager Regulatory Affairs

    1 week ago

    London, Greater London, United Kingdom i-Pharm Consulting Full time £60,000 - £100,000 per year

    Are you passionate about shaping regulatory strategy for life-changing therapies?Do you thrive in a fast-paced environment where your expertise drives global health outcomes?Are you ready to lead complex regulatory submissions and influence cross-functional teams?If your answer isyes, this opportunity could be perfect for you.Position: Senior Manager, Global...

  • Regulatory Affairs Manager

    3 days ago

    London, Greater London, United Kingdom The businesses of Merck KGaA, Darmstadt, Germany Full time

    Work Your Magic with us  Ready to explore, break barriers, and discover more? We know you've got big plans – so do we Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix...

  • Regulatory Risk Affairs Manager

    2 weeks ago

    London, Greater London, United Kingdom PIC Full time £60,000 - £100,000 per year

    Role purposeThe role is in the Regulatory Affairs team, which sits in the Risk and Compliance function.The role of the team is to facilitate strong regulatory risk management and ensure a good understanding of regulatory risks, issues and projects across PIC. The team assist the business in ensuring that regulatory risks and issues are considered as part of...

  • Regulatory Risk Affairs Manager

    2 weeks ago

    London, Greater London, United Kingdom Pension Insurance Corporation plc Full time £60,000 - £100,000 per year

    Role purposeThe role is in the Regulatory Affairs team, which sits in the Risk and Compliance function.The role of the team is to facilitate strong regulatory risk management and ensure a good understanding of regulatory risks, issues and projects across PIC.The team assist the business in ensuring that regulatory risks and issues are considered as part of...

  • Senior Regulatory Affairs Manager

    3 days ago

    London, Greater London, United Kingdom WEP Clinical Full time £60,000 - £120,000 per year

    Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring ideas that make a real difference. Be part of a...

  • Senior Regulatory Affairs Manager

    3 days ago

    London, Greater London, United Kingdom WEP Clinical Full time £60,000 - £120,000 per year

    Are you looking for an exciting and fulfilling new position? Join our dynamic team at WEP Clinical, where your contributions will play a key role in driving impactful solutions and improving outcomes for clients and patients. We encourage innovation and collaboration, challenging our team to bring ideas that make a real difference. Be part of a...

  • Global Regulatory Affairs Manager

    1 week ago

    London, Greater London, United Kingdom Novartis Full time £100,000 - £120,000 per year

    Job Description Summary#LI-Hybrid (12 days per month on-site)Location: London (The Westworks), United KingdomInternal Job Title: Global Program Regulatory ManagerWe are looking for an experienced and proactive Regulatory Affairs Manager to join our Global Regulatory Affairs team. This role is critical in driving regulatory strategy and managing operational...

  • Regulatory Affairs Biologics Consultant, Veterinary

    2 weeks ago

    London, Greater London, United Kingdom Coronado Research Full time £90,000 - £120,000 per year

    We are seeking an experienced freelance consultant specializing in Veterinary Regulatory Affairs with a strong background in biologics and immunology.The consultant will provide strategic and operational regulatory guidance to support the development, registration, and lifecycle management of veterinary biologic products, including vaccines, monoclonal...

  • Senior Director, Regulatory Affairs

    3 days ago

    London, Greater London, United Kingdom Beacon Therapeutics (USA) Inc Full time £150,000 - £200,000 per year

    Join Beacon Therapeutics (USA) Inc. as a Full-Time Senior Director of Regulatory Affairs and be at the forefront of transformative biotech innovations. This is a unique opportunity to shape regulatory strategies that directly influence the success of groundbreaking therapeutics in the UK market. Here, you will have the chance to leverage your expertise in a...