Remote Regulatory Affairs Manager – European CTAs
Remote Regulatory Affairs Manager – European CTAs

Remote Regulatory Affairs Manager – European CTAs

Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead the preparation and submission of Clinical Trial Applications across Europe.
  • Company: Dynamic consulting firm in the pharmaceutical industry.
  • Benefits: Fully remote work, flexible hours, and meaningful project contributions.
  • Why this job: Make a real difference in clinical trials while enjoying work-life balance.
  • Qualifications: Bachelor's degree in life sciences and experience in regulatory affairs.
  • Other info: 8+ month fixed-term contract with opportunities for growth.

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

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.

Remote Regulatory Affairs Manager – European CTAs employer: RBW Consulting

As a leading consulting firm in the pharmaceutical industry, we pride ourselves on fostering a flexible and inclusive work culture that empowers our employees to thrive. With opportunities for professional growth and the chance to contribute to impactful clinical projects, our remote Regulatory Affairs Manager role offers a unique advantage for those based in the UK or Sweden, ensuring a rewarding and meaningful career path.
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Contact Detail:

RBW Consulting Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Remote Regulatory Affairs Manager – European CTAs

Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn. Join relevant groups and engage in discussions to get your name out there and show off your expertise.

Tip Number 2

Prepare for virtual interviews by practising common questions related to clinical trials and regulatory submissions. We recommend setting up mock interviews with friends or using online platforms to boost your confidence.

Tip Number 3

Showcase your experience! When you get the chance to chat with potential employers, highlight specific projects you've worked on that relate to Clinical Trial Applications. This will help you stand out as a candidate who knows their stuff.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who take the initiative to connect directly with us.

We think you need these skills to ace Remote Regulatory Affairs Manager – European CTAs

Regulatory Affairs
Clinical Trial Applications (CTAs)
Experience in Clinical Trials
Bachelor's Degree in Life Science
Project Management
Attention to Detail
Communication Skills
Problem-Solving Skills
Knowledge of European Regulatory Guidelines
Remote Work Capability
Flexibility
Team Collaboration

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs and clinical trials. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory affairs and how your skills can contribute to our team. Keep it concise but impactful – we love a good story!

Showcase Your Knowledge: In your application, demonstrate your understanding of European Clinical Trial Applications. We’re looking for someone who knows the ins and outs of the process, so feel free to drop in some key terms or recent changes in regulations.

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 from our team. Plus, it’s super easy!

How to prepare for a job interview at RBW Consulting

Know Your Regulations

Make sure you brush up on the latest regulations regarding Clinical Trial Applications in Europe. Familiarise yourself with the specific requirements for different countries, as this will show your depth of knowledge and commitment to the role.

Showcase Your Experience

Prepare to discuss your previous experience in regulatory affairs, especially any relevant projects you've led. Use specific examples to illustrate how you've successfully navigated challenges in clinical trials, as this will demonstrate your capability and confidence.

Ask Insightful Questions

Come prepared with questions that show your interest in the company and the role. Inquire about their current projects or challenges they face in regulatory affairs. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.

Highlight Your Flexibility

Since this role offers flexible working, be ready to discuss how you manage your time and work effectively in a remote setting. Share strategies you use to stay organised and productive, which will reassure them of your ability to thrive in a fully remote environment.

Remote Regulatory Affairs Manager – European CTAs
RBW Consulting

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