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- Tasks: Support and manage pharmaceutical product portfolios while ensuring compliance with UK regulations.
- Company: Join a leading global healthcare provider dedicated to innovative solutions.
- Benefits: Competitive pay, hybrid work model, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by working on life-saving innovations.
- Qualifications: Relevant scientific degree or equivalent experience in regulatory affairs.
- Other info: Collaborative environment with excellent career advancement potential.
The predicted salary is between 52000 - 62400 £ per year.
CK Group are recruiting for a Regulatory Affairs Associate to join a leading global healthcare company on a contract basis until December 2026. This is a hybrid role with 2 days per week in Reading.
Salary: From £25 ph PAYE
Regulatory Affairs Associate Role:
- Support and maintain pharmaceutical product portfolios
- Manage ongoing product information updates
- Support regulatory project plan execution
- Assist in the preparation and review of labelling and local SOPs
- Compile regulatory documents for submission
Your Background:
- Hold a relevant scientific degree or have equivalent working experience
- Good knowledge and experience of UK regulations
- Previous working experience in pharmaceutical regulatory affairs
- Ability and experience to work cross-functionally with different functions involved: Global functions, QA, PV, Marketing
- Excellent communication skills
- Any project management experience would be an advantage
Company:
Our client is one of the world's leading healthcare providers, and has been highly innovative in providing healthcare solutions to unmet medical needs through scientific advancement as well as strategic acquisitions and partnerships. They work at the critical intersection where innovations that save and sustain lives meet the physicians, nurses and pharmacists who make it happen. Our client is committed to improving outcomes for patients, and helping their partners meet the evolving challenges and opportunities in healthcare around the world.
Apply: For more information, or to apply for this Regulatory Affairs Associate please contact the Key Accounts Team. It is essential that applicants hold entitlement to work in the UK. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Regulatory Affairs Associate employer: CK Group- Science, Clinical and Technical
Contact Detail:
CK Group- Science, Clinical and Technical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Associate
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on UK regulations and your past experiences. We recommend practising common interview questions with a friend or in front of a mirror to boost your confidence.
✨Tip Number 3
Showcase your project management skills! Even if you don’t have formal experience, think about times you’ve led projects or coordinated tasks. We want to see how you can bring that to the table.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we’re always looking for passionate candidates who are ready to make an impact in healthcare.
We think you need these skills to ace Regulatory Affairs Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant scientific degree and any experience in pharmaceutical regulatory affairs. 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 passionate about regulatory affairs and how your previous experiences make you a great fit for our team. Keep it concise but impactful!
Showcase Communication Skills: Since excellent communication is key for this role, make sure to demonstrate your ability to convey complex information clearly in your application. We love seeing candidates who can communicate effectively across different functions.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at CK Group- Science, Clinical and Technical
✨Know Your Regulations
Make sure you brush up on UK regulations related to pharmaceutical products. Being able to discuss specific regulations and how they apply to the role will show that you're not just familiar with the basics, but that you’re ready to hit the ground running.
✨Showcase Your Cross-Functional Experience
Since this role involves working with various teams, be prepared to share examples of how you've successfully collaborated across different functions in your previous roles. Highlighting your ability to communicate effectively with QA, PV, and Marketing will set you apart.
✨Prepare for Project Management Questions
Even if project management isn't a core part of the job, having some experience in this area can be beneficial. Think of instances where you managed timelines or coordinated tasks, and be ready to discuss these experiences during the interview.
✨Practice Your Communication Skills
Excellent communication is key in regulatory affairs. Practise articulating complex information clearly and concisely. You might even want to do a mock interview with a friend to get comfortable discussing your background and the role's requirements.
