At a Glance
- Tasks: Lead regulatory strategy and submissions across multiple regions for a growing pharmaceutical company.
- Company: Join Clinigen, a dynamic global specialty pharmaceutical services business with exciting growth opportunities.
- Benefits: Enjoy 27 days holiday, a bonus scheme, pension contributions, and flexible benefits.
- Why this job: Make a real impact in regulatory affairs while collaborating with diverse teams and partners.
- Qualifications: Bachelor's degree in Life Sciences and strong experience in international regulatory environments required.
- Other info: Fast-paced environment with excellent career growth and recognition opportunities.
The predicted salary is between 36000 - 60000 £ per year.
Clinigen is a rapidly growing global specialty pharmaceutical services business with a unique combination of services across the pharmaceutical lifecycle. We currently have over 1,000 employees headquartered in the UK with global offices in the US, EU (Belgium, Germany, France), Asia Pacific and South Africa. Clinigen is growing rapidly and is positioned well for an exciting future of continued expansion.
To support our growth, we are seeking a dynamic, detail orientated and collaborative Regulatory Affairs Manager. In this role, you will be responsible for leading and coordinating regulatory strategy, submissions and compliance activities across multiple regions. You will ensure that products meet the regulatory requirements and maintain compliance throughout the product lifecycle. You will act as a key liaison between internal teams, regulatory authorities and external partners. This is a dedicated Regulatory Affairs Manager role supporting Colonis, a Clinigen Group company.
You will sit within the wider Regulatory Affairs team and will work very closely with the Regulatory Affairs Director for Colonis. You will also collaborate closely with Colonis commercial teams, working hand-in-hand as commercial agreements are established with partners and alongside Supply Chain and Quality functions. The role involves broad interaction across the Colonis organisation, attendance at regular cross-functional meetings and ongoing reporting on regulatory activities.
Key Responsibilities:- Develop and implement regulatory strategies for product registration and maintenance in international markets.
- Prepare, review, and submit regulatory documents to health authorities across multiple regions (e.g. LATAM, MENA).
- Provide responses to regulatory authority queries and ensure timely approvals.
- Oversee product labelling, packaging, and promotional material compliance with local regulations.
- Conduct regulatory reviews and provide due diligence reports.
- Identify and mitigate regulatory risks impacting product launches or market continuity.
- Act as the primary contact with regulatory agencies, distributors, and consultants in international markets.
- Interact with Quality, Supply Chain, Commercial and Project teams to align regulatory requirements with business objectives.
- Submit variations, renewals and PSUR’s for existing products.
- Engage directly with regulatory authorities, including participation in agency meetings.
The role requires someone with hands-on experience managing regulatory submissions in MENA markets independently, without relying solely on partner support. You will be comfortable working with incomplete or evolving information, have submitted in these regions multiple times, and understand regulatory expectations well enough to anticipate agency questions, reducing reactive firefighting and improving submission efficiency.
Key Requirements:- Bachelor's Degree (or preferably higher degree) in Life Sciences or scientific discipline.
- Experience within the pharmaceutical industry.
- Must have strong experience in international regulatory environments, with particular emphasis on the MENA region, especially Qatar, UAE and Saudi Arabia. South American regulatory experience would also be advantageous (not essential).
- Proven ability to successfully manage regulatory submissions.
- Strong operational regulatory background required.
- Experience within a service provider environment is desirable but not essential.
- Excellent organisational and project management skills.
- Outstanding written, verbal and interpersonal communications skills.
- Excellent ability to handle multiple tasks in a fast-paced and constantly changing environment.
- 27 days holiday plus bank holidays.
- Discretionary Bonus Scheme.
- Pension contributions 4.5% matched.
- Life assurance 4 x annual salary.
- Flexible Benefits Platform with £25/month Company contribution.
- Annual salary review.
- Independent financial advice service.
- Enhanced Employee Assistance Programme.
- Shopping discounts with retailers.
- Long service awards.
- Recognition scheme.
Regulatory Affairs Manager employer: Clinigen
Contact Detail:
Clinigen Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager
✨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 when it comes to landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory requirements, especially in the MENA region. We recommend practising common interview questions and having examples ready that showcase your experience with submissions and compliance.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your values and career goals. At StudySmarter, we encourage you to check out our website for openings that match your skills and aspirations in regulatory affairs.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. We believe that keeping the lines of communication open can help you stand out from the crowd.
We think you need these skills to ace Regulatory Affairs Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Manager role. Highlight your experience in international regulatory environments, especially in the MENA region, and showcase any relevant achievements that align with the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for Clinigen. Mention your hands-on experience with regulatory submissions and how you can contribute to the team’s success.
Showcase Your Communication Skills: Since this role involves liaising with various teams and regulatory authorities, make sure to demonstrate your outstanding written and verbal communication skills in your application. Clear and concise language goes a long way!
Apply Through Our Website: We encourage you to apply through our website for a smoother application 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 Clinigen
✨Know Your Regulatory Stuff
Make sure you brush up on the latest regulations, especially in the MENA region. Familiarise yourself with the specific requirements for countries like Qatar, UAE, and Saudi Arabia. Being able to discuss these in detail will show that you're not just a candidate, but a potential asset to their regulatory team.
✨Showcase Your Project Management Skills
Since this role involves juggling multiple tasks, be ready to share examples of how you've successfully managed projects in the past. Highlight your organisational skills and how you’ve handled tight deadlines or complex submissions. This will demonstrate your ability to thrive in a fast-paced environment.
✨Prepare for Agency Interactions
Think about your experiences interacting with regulatory authorities. Be prepared to discuss how you've navigated agency meetings and responded to queries. This will help illustrate your hands-on experience and your ability to act as a key liaison, which is crucial for this role.
✨Collaborative Mindset is Key
This position requires working closely with various teams, so be ready to talk about your collaborative experiences. Share instances where you’ve worked with commercial, quality, or supply chain teams to align regulatory strategies with business objectives. This will show that you’re a team player who can integrate well into their culture.