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- Tasks: Lead regulatory strategy and lifecycle management for innovative medicines.
- Company: Join a global biopharmaceutical leader focused on patient-first solutions.
- Benefits: Competitive salary, dynamic work environment, and opportunities for professional growth.
- Why this job: Make a real impact in healthcare by driving regulatory success.
- Qualifications: Degree in Life Sciences and significant Regulatory Affairs experience required.
- Other info: Collaborative team culture with a focus on innovation and excellence.
The predicted salary is between 60000 - 80000 £ per year.
Apsida Life Science are currently partnering with a global biopharmaceutical company recognised for developing innovative medicines that address complex and serious diseases. The organisation combines strong scientific expertise with a patient-first approach, focusing on improving standards of care through breakthrough therapies and close collaboration with healthcare systems. They are seeking a Senior Regulatory Project Manager to support their UK portfolio.
Location: M4 Corridor
As a key member of the Regulatory team, you will act as the primary contact for assigned products, driving regulatory strategy, lifecycle management, and Health Authority interactions, with a strong focus on MHRA engagement.
Responsibilities:
- Act as the primary Regulatory contact for an assigned product portfolio.
- Lead lifecycle management activities, including variations, clinical trials and paediatric investigation plans.
- Develop and execute regulatory strategies and timelines aligned with global and UK objectives.
- Serve as the main liaison with the MHRA, supporting Health Authority interactions and meetings.
- Ensure timely preparation and submission of Marketing Authorisations and other regulatory filings.
- Collaborate cross-functionally with Brand, Affiliate, and Area Regulatory teams.
- Support product launches, acquisitions, and divestitures from a regulatory perspective.
Requirements:
- Degree in Life Sciences or a related field.
- Significant experience within Regulatory Affairs in the pharmaceutical industry.
- Strong understanding of UK regulatory processes and MHRA interactions.
- Experience managing regulatory submissions and lifecycle activities.
- Ability to manage multiple priorities and work both independently and collaboratively.
If you are interested in learning more, please reach out to Geneva Jones at Apsida Life Science: www.apsida.co.uk +44(0)7441341762
Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK) & Boston (USA) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.
Senior Regulatory Project Manager in Slough employer: Apsida Life Science
Contact Detail:
Apsida Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Project Manager in Slough
✨Tip Number 1
Network like a pro! Reach out to your connections in the biopharmaceutical industry, especially those who have experience with regulatory affairs. A friendly chat can lead to valuable insights and even job leads.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of UK regulatory processes and MHRA interactions. We recommend practising common interview questions and scenarios related to lifecycle management and regulatory strategy.
✨Tip Number 3
Showcase your expertise! During interviews, be ready to discuss specific examples of how you've successfully managed regulatory submissions or collaborated with cross-functional teams. This will demonstrate your hands-on experience.
✨Tip Number 4
Don’t forget to apply through our website! It’s a great way to ensure your application gets noticed. Plus, we’re always looking for talented individuals like you to join our network in the life sciences sector.
We think you need these skills to ace Senior Regulatory Project Manager in Slough
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Regulatory Project Manager role. Highlight your experience in regulatory affairs, especially with UK processes and MHRA interactions. We want to see how your background aligns with the responsibilities listed in the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your skills can contribute to the team. We love seeing candidates who can connect their experiences to our patient-first approach.
Showcase Your Achievements: When detailing your experience, focus on specific achievements rather than just duties. Did you lead a successful regulatory submission? Share those details! We appreciate candidates who can demonstrate their impact in previous roles.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss any important updates from us!
How to prepare for a job interview at Apsida Life Science
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of UK regulatory processes and MHRA interactions. Familiarise yourself with recent changes in regulations and be ready to discuss how they might impact the products you'll be managing.
✨Showcase Your Project Management Skills
Prepare examples that highlight your experience in lifecycle management and regulatory submissions. Be ready to explain how you've successfully managed multiple priorities in past roles, as this will demonstrate your ability to handle the demands of the Senior Regulatory Project Manager position.
✨Engage with the Patient-First Approach
Since the company focuses on a patient-first approach, think about how your work in regulatory affairs can directly impact patient care. Be prepared to discuss how you can contribute to improving standards of care through your role.
✨Collaborate and Communicate
As a key member of the Regulatory team, you'll need to work cross-functionally. Prepare to talk about your experience collaborating with different teams and how you ensure effective communication, especially when liaising with Health Authorities like the MHRA.