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- Tasks: Manage regulatory submissions and liaise with health authorities for timely approvals.
- Company: Join a rapidly growing consultancy serving top multinational pharmaceutical companies.
- Benefits: Enjoy a part-time, fully remote role outside IR35 with flexible hours.
- Why this job: Be part of a dynamic team making a real impact in the pharmaceutical industry.
- Qualifications: Must have UK and Ireland regulatory experience, especially post-Brexit IRP knowledge.
- Other info: This is a 12-month contract, perfect for those looking to balance work and studies.
The predicted salary is between 36000 - 60000 £ per year.
Regulatory Affairs Manager – UK and Ireland outside IR35, part-time, remote
Your new companyThis rapidly growing Regulatory Affairs consultancy is looking for an experienced Regulatory Affairs Manager who specialises in UK and Ireland registrations to fulfil a 12-month, remote contract which is outside IR35.They count some of the biggest multinational pharmaceutical companies as clients and contin…
Regulatory Affairs Consultant Uk and Ire outside IR35 employer: Hays
Contact Detail:
Hays Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Consultant Uk and Ire outside IR35
✨Tip Number 1
Familiarise yourself with the latest regulatory guidelines and changes in the UK and Ireland. Being up-to-date will not only boost your confidence but also demonstrate your commitment to the role during any discussions.
✨Tip Number 2
Network with professionals in the Regulatory Affairs field, especially those who have experience with the MHRA and HPRA. Engaging in conversations can provide insights and potentially lead to referrals that could strengthen your application.
✨Tip Number 3
Prepare to discuss specific examples of your past experiences with regulatory submissions and health authority interactions. Highlighting your hands-on experience will show that you can hit the ground running in this fast-paced environment.
✨Tip Number 4
Research the consultancy's current projects and clients. Understanding their work will allow you to tailor your conversation and show how your skills align with their needs, making you a more attractive candidate.
We think you need these skills to ace Regulatory Affairs Consultant Uk and Ire outside IR35
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs, particularly with UK and Ireland registrations. Emphasise any relevant post-Brexit experience and specific projects you've worked on that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that directly addresses the requirements of the role. Mention your familiarity with MHRA and HPRA submissions, and how your skills can contribute to the consultancy's success. Be sure to convey your enthusiasm for the position.
Showcase Relevant Skills: In your application, highlight key skills such as regulatory submissions, health authority interactions, and labelling management. Use specific examples to demonstrate your expertise and how you have successfully navigated similar challenges in the past.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or inconsistencies. A polished application reflects your attention to detail, which is crucial in regulatory affairs.
How to prepare for a job interview at Hays
✨Showcase Your Regulatory Knowledge
Make sure to brush up on your knowledge of UK and Ireland regulatory frameworks, especially post-Brexit changes. Be prepared to discuss specific regulations and how they impact submissions to the MHRA and HPRA.
✨Demonstrate Your Experience
Highlight your previous experience with regulatory submissions and health authority interactions. Use specific examples to illustrate how you've successfully managed applications, variations, and renewals in the past.
✨Prepare for Scenario Questions
Expect scenario-based questions that assess your problem-solving skills. Think about potential challenges you might face in this role and how you would address them, particularly regarding labelling updates and compliance.
✨Communicate Clearly and Confidently
Since this role involves liaising with health authorities and internal teams, practice clear and confident communication. Be ready to explain complex regulatory concepts in a straightforward manner, showcasing your ability to collaborate effectively.