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For Companies At a Glance
- Tasks: Manage regulatory submissions and health authority interactions for the UK and Ireland.
- Company: Join a rapidly growing consultancy serving top multinational pharmaceutical companies.
- Benefits: Enjoy a part-time, fully remote role with flexible hours outside IR35.
- Why this job: Be part of a dynamic team making a real impact in the pharmaceutical industry.
- Qualifications: Must have a strong regulatory background and post-Brexit IRP experience.
- 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.
Job Description
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…
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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 regulations and guidelines from the MHRA and HPRA. Being up-to-date with current practices 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 post-Brexit regulations. 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 direct involvement in successful applications will showcase your expertise and readiness for the role.
✨Tip Number 4
Research the consultancy's clients and their recent projects. 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 regulatory 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 Expertise
Make sure to highlight your experience with UK and Ireland regulatory submissions, especially your familiarity with the MHRA and HPRA processes. Be prepared to discuss specific examples of past submissions and how you managed post-submission queries.
✨Demonstrate Your Knowledge of Recent Changes
Stay updated on recent regulatory changes post-Brexit, particularly regarding the International Recognition Procedure (IRP). Discuss how these changes impact regulatory affairs and how you've adapted your strategies accordingly.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills in regulatory affairs. Think about challenges you've faced in previous roles and how you successfully navigated them, particularly in labelling and product information management.
✨Emphasise Collaboration Skills
Since the role involves liaising with health authorities and collaborating with internal teams, be ready to discuss your teamwork experiences. Highlight how you ensure compliance and accuracy while working with diverse stakeholders.