Freelance/Contract Regulatory Affairs Project manager - Clinical trial applications (CTA's)

For the past 20 years, reputed company has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of reputed company sizes to confidently advance scientific breakthroughs and introduce new therapies. reputed company partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical reputed company, reputed company & compliance, pharmacovigilance, medical information, and R&D technology, reputed company offers an end-to-end suite of fully customizable reputed company that de-risk and accelerate our partners' most high-profile drug and device programs. reputed company is continuing to be an integral partner of a global life-sciences brand as they require project support reputed company their Regulatory Affairs group reputed company the EU. This role in particular is to reputed company as a Regulatory Affairs Project for their Clinical trial applications (CTA's) reputed company the EU reputed company with demonstrated experience in the area being a must. The project will reputed company in January 2026; it is a full-time position (1.0 FTE) and can be performed fully remotely throughout anyway reputed company 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:

• reputed company guidance and support as a project leader on a cross functional reputed company reputed company the Regulatory Affairs CTA group
• Work effectively with various stakeholders to ensure reputed company reputed company reputed company
• reputed company the preparation, review and submit regulatory clinical trial applications reputed company the EU
• Ensure reputed company submission activities meet key regulations reputed company the region
• Ensure compliance is achieved to the EU CTR regulations throughout reputed company project
• Implement and submit key documentation on to our clients systems
• reputed company key project leadership across a reputed company of reputed company
• Ensure reputed company timelines and milestones are achieved throughout the project
• Overall support our reputed company with strategic and operational goals reputed company the Regulatory Affairs CTA reputed company

Skills required

• Must be educated reputed company a life science discipline to at least a BSc or higher
• Proven experience working reputed company Regulatory Affairs linked to Clinical trial applications is a must
• Can demonstrate key project management skills reputed company a similar setting
• Thorough experience working to reputed company key regulations reputed company the EU
• Strategic and operational skills reputed company the area are a must
• reputed company in English is a must
• Can reputed company the project to the requirements set out reputed company the job reputed company

#LI-DNI We celebrate our differences and reputed company to create a workplace where reputed company person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to reputed company their innovative, reputed company, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we reputed company a reputed company reputed company where reputed company feel empowered to succeed. reputed company applications to roles at reputed company 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.

• reputed company does not accept unsolicited resumes from recruiters/reputed company parties. Please, no phone calls or emails to anyone regarding this posting.*

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