Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Lead clinical regulatory intelligence projects and collaborate with clients to drive success.
- Company: Leading pharmaceutical company focused on innovation and excellence.
- Benefits: Competitive daily rate, fully remote work, and a 12-month contract.
- Why this job: Make a real impact in the pharma industry while working flexibly from anywhere.
- Qualifications: 4+ years in pharma consulting, strong regulatory affairs knowledge, and Agile experience.
- Other info: Join a dynamic team and enhance your career in a rapidly evolving field.
The predicted salary is between 28000 - 42000 £ per year.
Leading pharmaceutical company require a consultant to help with clinical regulatory intelligence.
- Skills:
- Regulatory Intelligence platforms
- Agile BA
- Regulatory Affairs/Operations
- Submissions
- eCTD
- CMC Experience
59 years experience (4+ minimum) in pharma/life sciences consulting or delivery.
- Regulatory Affairs / Regulatory Operations experience
- Hands-on work with Regulatory Intelligence platforms
- Strong exposure to eCTD, submissions, labeling, CMC variations
- Understanding of Regulatory Intelligence lifecycle (capture – curate – consume)
- Ability to independently lead a workstream and work directly with client stakeholders
- Business Analysis / Consulting skills
- Requirements gathering
- User stories
- Gap analysis & future-state design
- Agile delivery experience (mandatory)
- Experience with SaaS platform implementations
- Strong communication and stakeholder-management skills
This is a fully remote contract offering £350 per day for a 12 month contract, outside of IR35. Ideally start within 2 weeks of offer (end Jan).
Clinical Regulatory Intelligence Analyst / Consultant employer: Escritor y articulista
Contact Detail:
Escritor y articulista Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Regulatory Intelligence Analyst / Consultant
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharma and life sciences sectors. Let them know you're on the lookout for opportunities, especially in clinical regulatory intelligence. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Show off your skills! Prepare a portfolio or a case study that highlights your experience with regulatory intelligence platforms and eCTD submissions. This will give potential employers a clear picture of what you bring to the table.
✨Tip Number 3
Practice makes perfect! Get ready for interviews by rehearsing common questions related to regulatory affairs and Agile delivery. We recommend doing mock interviews with friends or using online platforms to boost your confidence.
✨Tip Number 4
Apply through our website! We’ve got loads of opportunities that match your skills. Don’t just wait for the right job to come to you; take the initiative and submit your application directly through us!
We think you need these skills to ace Clinical Regulatory Intelligence Analyst / Consultant
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in Regulatory Affairs and Operations. We want to see how your skills align with the job description, so don’t be shy about showcasing your hands-on work with Regulatory Intelligence platforms and eCTD submissions.
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 role. Mention your Agile delivery experience and how you’ve successfully led workstreams in the past. Let us know how you can add value to our team!
Showcase Your Communication Skills: Strong communication is key in this role. In your application, highlight examples where you've effectively managed stakeholders or gathered requirements. We love seeing how you can bridge the gap between technical details and client needs.
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. Plus, we love seeing candidates who take that extra step!
How to prepare for a job interview at Escritor y articulista
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of regulatory intelligence platforms and the eCTD process. Be ready to discuss your hands-on experience with submissions and CMC variations, as this will show that you’re not just familiar with the theory but have practical insights to share.
✨Show Off Your Agile Skills
Since Agile delivery experience is a must, prepare to talk about specific projects where you’ve successfully implemented Agile methodologies. Think about how you gathered requirements, created user stories, and conducted gap analysis. Real examples will make your experience stand out!
✨Communicate Like a Pro
Strong communication and stakeholder management skills are key for this role. Practice articulating your thoughts clearly and confidently. You might even want to prepare a few scenarios where you effectively managed client relationships or led a workstream independently.
✨Research the Company
Before the interview, take some time to research the pharmaceutical company you’re applying to. Understand their products, recent news, and their approach to regulatory affairs. This will not only help you tailor your answers but also demonstrate your genuine interest in the role and the company.
