EU Regulatory Affairs Project Lead - Clinical Trial Apps
EU Regulatory Affairs Project Lead - Clinical Trial Apps

EU Regulatory Affairs Project Lead - Clinical Trial Apps

Full-Time 36000 - 60000 £ / year (est.) Home office possible
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At a Glance

  • Tasks: Lead projects for Clinical trial applications and ensure compliance with EU regulations.
  • Company: Dynamic life sciences consulting firm focused on innovation.
  • Benefits: Remote work, competitive salary, and opportunities for career advancement.
  • Why this job: Make a real impact in the life sciences field while working remotely.
  • Qualifications: BSc in Life Sciences and experience in Regulatory Affairs required.
  • Other info: Project starts in January 2026 with potential for extension.

The predicted salary is between 36000 - 60000 £ per year.

A life sciences consulting firm is seeking a Regulatory Affairs Project leader to oversee Clinical trial applications in the EU. This full-time remote role requires a BSc in Life Sciences and proven experience in Regulatory Affairs.

The individual will guide project teams, ensure compliance with EU regulations, and support strategic goals. Candidates with strong project management skills and fluency in English are encouraged to apply. The project starts in January 2026 and has potential for extension.

EU Regulatory Affairs Project Lead - Clinical Trial Apps employer: ProPharma Group

As a leading life sciences consulting firm, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. With a strong focus on professional development, we offer numerous growth opportunities and support for continuous learning, ensuring that our team members are well-equipped to navigate the complexities of EU regulatory affairs. Our remote work model provides flexibility, allowing you to balance your professional and personal life while contributing to impactful projects in the healthcare sector.
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Contact Detail:

ProPharma Group Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land EU Regulatory Affairs Project Lead - Clinical Trial Apps

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs space on LinkedIn. Join relevant groups and engage in discussions to get your name out there and learn about potential opportunities.

✨Tip Number 2

Prepare for interviews by brushing up on EU regulations and recent changes in clinical trial applications. We want you to be the go-to expert in the room, so show off your knowledge and confidence!

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you and match your skills, making your application stand out.

✨Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. It keeps you fresh in their minds and demonstrates your professionalism.

We think you need these skills to ace EU Regulatory Affairs Project Lead - Clinical Trial Apps

Regulatory Affairs
Clinical Trial Applications
Project Management
Compliance with EU Regulations
BSc in Life Sciences
Fluency in English
Strategic Planning
Team Leadership

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in Regulatory Affairs and any relevant projects you've led. We want to see how your background aligns with the role, so don’t be shy about showcasing your skills!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re the perfect fit for the EU Regulatory Affairs Project Lead role. We love seeing enthusiasm and a clear understanding of the position.

Showcase Your Project Management Skills: Since this role involves guiding project teams, make sure to highlight your project management experience. We’re looking for examples of how you’ve successfully led projects in the past, especially in the life sciences field.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates regarding the role!

How to prepare for a job interview at ProPharma Group

✨Know Your Regulations

Make sure you brush up on the latest EU regulations regarding clinical trial applications. Being able to discuss specific regulations and how they impact project management will show that you're not just familiar with the field, but that you’re also proactive in staying updated.

✨Showcase Your Project Management Skills

Prepare examples from your past experiences where you successfully led projects, particularly in regulatory affairs. Use the STAR method (Situation, Task, Action, Result) to structure your answers, highlighting how your leadership contributed to compliance and strategic goals.

✨Demonstrate Team Leadership

Since this role involves guiding project teams, be ready to discuss your leadership style. Share instances where you motivated a team or resolved conflicts, emphasising your ability to foster collaboration and ensure everyone is aligned with project objectives.

✨Practice Your English Fluency

As fluency in English is crucial, consider doing mock interviews or discussions in English. This will help you articulate your thoughts clearly and confidently during the actual interview, making a strong impression on the interviewers.

EU Regulatory Affairs Project Lead - Clinical Trial Apps
ProPharma Group
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  • EU Regulatory Affairs Project Lead - Clinical Trial Apps

    Full-Time
    36000 - 60000 £ / year (est.)
  • P

    ProPharma Group

    100-200
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