Remote Clinical Regulatory Intelligence Consultant
Remote Clinical Regulatory Intelligence Consultant

Remote Clinical Regulatory Intelligence Consultant

Freelance 70000 - 105000 £ / year (est.) Home office possible
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At a Glance

  • Tasks: Lead workstreams and gather requirements in clinical regulatory intelligence.
  • Company: Top-tier pharmaceutical company with a focus on innovation.
  • Benefits: £350 per day, fully remote work, and a 12-month contract.
  • Why this job: Make a significant impact in the pharma industry while working from anywhere.
  • Qualifications: 4+ years in pharma consulting and expertise in Regulatory Affairs.
  • Other info: Start within two weeks and enjoy a flexible work environment.

The predicted salary is between 70000 - 105000 £ per year.

A leading pharmaceutical company is seeking a consultant to assist with clinical regulatory intelligence. This role requires a minimum of 4 years of experience in pharma consulting and expertise in Regulatory Affairs and Operations.

The consultant will work fully remote, leading workstreams, gathering requirements, and utilizing Regulatory Intelligence platforms.

This position offers £350 per day on a 12-month contract, outside of IR35, ideally starting within two weeks of offer.

Remote Clinical Regulatory Intelligence Consultant employer: Escritor y articulista

As a leading pharmaceutical company, we pride ourselves on fostering a dynamic and inclusive work culture that prioritises employee growth and development. Our fully remote position for a Clinical Regulatory Intelligence Consultant not only offers competitive compensation but also provides the flexibility to balance work and personal life while contributing to impactful projects in the healthcare sector. Join us to be part of a team that values innovation, collaboration, and the pursuit of excellence in regulatory affairs.
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Contact Detail:

Escritor y articulista Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Remote Clinical Regulatory Intelligence Consultant

✨Tip Number 1

Network like a pro! Reach out to your connections in the pharma industry and let them know you're on the lookout for opportunities. You never know who might have a lead or can put in a good word for you.

✨Tip Number 2

Prepare for virtual interviews by setting up a professional backdrop and testing your tech. We want to make sure you shine during those online chats, so practice answering common questions related to Regulatory Affairs and Operations.

✨Tip Number 3

Showcase your expertise! Create a portfolio or a presentation that highlights your past projects and successes in clinical regulatory intelligence. This will help you stand out and demonstrate your value to potential employers.

✨Tip Number 4

Don't forget to apply through our website! We’ve got loads of opportunities waiting for you, and applying directly can give you an edge. Plus, it’s super easy to keep track of your applications!

We think you need these skills to ace Remote Clinical Regulatory Intelligence Consultant

Regulatory Affairs
Regulatory Operations
Pharma Consulting
Workstream Leadership
Requirements Gathering
Regulatory Intelligence Platforms
Remote Work Skills
Project Management

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in pharma consulting and Regulatory Affairs. We want to see how your skills align 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 the perfect fit for this remote role. Share specific examples of how you've led workstreams or gathered requirements in past positions.

Showcase Your Regulatory Intelligence Skills: Since this role involves using Regulatory Intelligence platforms, make sure to mention any tools or systems you’ve worked with. We love seeing candidates who are familiar with the latest tech in the 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 during the process!

How to prepare for a job interview at Escritor y articulista

✨Know Your Regulatory Affairs Inside Out

Make sure you brush up on your knowledge of Regulatory Affairs and Operations. Be prepared to discuss specific regulations, guidelines, and how they apply to clinical trials. This will show that you’re not just familiar with the basics but have a deep understanding of the field.

✨Demonstrate Your Consulting Experience

Since the role requires a minimum of 4 years in pharma consulting, be ready to share concrete examples from your past experiences. Highlight projects where you led workstreams or gathered requirements, and explain how your contributions made a difference.

✨Familiarise Yourself with Regulatory Intelligence Platforms

Research the specific Regulatory Intelligence platforms that the company uses. If you have experience with similar tools, be sure to mention it. If not, showing that you’ve done your homework and understand their importance can set you apart.

✨Prepare Questions That Show Your Interest

Think of insightful questions to ask during the interview. This could be about the company's approach to regulatory challenges or how they envision the consultant's role evolving. It shows you’re engaged and genuinely interested in contributing to their success.

Remote Clinical Regulatory Intelligence Consultant
Escritor y articulista
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