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- Tasks: Lead regulatory strategy and manage submissions for biotech products.
- Company: Join a well-known biotech with a strong global presence.
- Benefits: Enjoy flexible working options and potential contract extension.
- Why this job: Make an impact in global regulatory affairs while collaborating with diverse teams.
- Qualifications: Prior experience in regulatory affairs for marketing applications and clinical trials is essential.
- Other info: This is a 12-month contract role with opportunities for growth.
The predicted salary is between 54000 - 84000 £ per year.
Global Regulatory Affairs Manager – contract jobYour new companyThis well-known biotech is looking for an experienced Regulatory Affairs Manager to join their established Global Regulatory Affairs team. This is a 12-month contract job with scope for extension.Your new roleAs Global Regulatory Affairs Manager you will support the creation of strategy and execution plans and manage regulatory submissions (e.g., clinical trial and marketing applications) for products within the portfolio in compliance with global filing plans and local regulatory requirements.As Global Regulatory Affairs Manager, you will take a lead role in advising the Global Regulatory team on regional considerations in developing strategy, as well as ensuring the regional needs are well-defined and implemented in collaboration with relevant regional stakeholders.What you’ll need to succeedIn order to be considered for this contract job as Regulatory Affairs Manager Global, you must have prior experience in region for MAs, CTAs / post approval changes and amendments, extensions, and renewals.What you’ll get in returnFlexible working options are available.What you need to do nowFor more information on this or any other Regulatory Affairs contract jobs, please apply to this advertisement. …
Regulatory Affairs Senior Manager EU employer: Hays Specialist Recruitment Limited
Contact Detail:
Hays Specialist Recruitment Limited Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Senior Manager EU
✨Tip Number 1
Familiarize yourself with the specific regulatory requirements in the EU. Understanding the nuances of the European Medicines Agency (EMA) guidelines will give you an edge when discussing your experience and strategies during the interview.
✨Tip Number 2
Network with professionals in the biotech and regulatory affairs sectors. Attend industry conferences or webinars to connect with others who may have insights into the company or role, which can help you tailor your approach.
✨Tip Number 3
Prepare to discuss specific examples from your past experiences where you successfully managed regulatory submissions. Highlighting your achievements in clinical trial applications and marketing authorizations will demonstrate your capability for this role.
✨Tip Number 4
Stay updated on current trends and changes in regulatory affairs within the biotech industry. Being knowledgeable about recent developments will show your commitment to the field and your proactive approach to the role.
We think you need these skills to ace Regulatory Affairs Senior Manager EU
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Regulatory Affairs Senior Manager position. Understand the key responsibilities and required qualifications to tailor your application accordingly.
Highlight Relevant Experience: In your CV and cover letter, emphasize your prior experience with marketing applications, clinical trial applications, and any post-approval changes. Use specific examples to demonstrate your expertise in regulatory affairs.
Showcase Strategic Thinking: Since the role involves creating strategy and execution plans, include examples of how you have successfully developed and implemented regulatory strategies in previous positions.
Tailor Your Application: Customize your cover letter to reflect your understanding of the company's needs and how your background aligns with their goals. Mention your ability to collaborate with regional stakeholders and adapt to local regulatory requirements.
How to prepare for a job interview at Hays Specialist Recruitment Limited
✨Understand Regulatory Frameworks
Make sure you have a solid grasp of the regulatory frameworks relevant to the biotech industry, especially in the EU. Be prepared to discuss how these regulations impact product submissions and what strategies you would implement to ensure compliance.
✨Showcase Your Experience
Highlight your previous experience with marketing applications, clinical trial applications, and post-approval changes. Use specific examples to demonstrate your expertise and how it aligns with the requirements of the role.
✨Collaborative Mindset
Emphasize your ability to work collaboratively with regional stakeholders. Discuss any past experiences where you successfully navigated cross-functional teams to achieve regulatory goals.
✨Prepare for Scenario Questions
Anticipate scenario-based questions that assess your problem-solving skills in regulatory affairs. Think about challenges you've faced in the past and how you overcame them, particularly in relation to compliance and strategy execution.
