At a Glance
- Tasks: Develop regulatory strategies and manage submissions for oncology drug development.
- Company: Join Regeneron, a leader in advancing science and medicine.
- Benefits: Comprehensive benefits including health programs, fitness centres, and equity awards.
- Why this job: Make a meaningful impact on patients' lives while collaborating with global experts.
- Qualifications: Advanced degree and 4+ years of regulatory experience in clinical development.
- Other info: Inclusive culture with excellent growth opportunities and a focus on innovation.
The predicted salary is between 43200 - 72000 £ per year.
Overview
At Regeneron, we’re advancing science and medicine to improve lives. We’re seeking a talented Regulatory Affairs Manager to join our team and play a pivotal role in supporting EU regulatory activities for oncology drug development. This is your chance to contribute to groundbreaking clinical development programs while collaborating with global experts and building relationships across the EU regulatory network. Join us in shaping the future of oncology treatments and making a meaningful impact on patients’ lives.
Responsibilities
- Developing regulatory strategies for oncology programs by researching guidelines, EU precedents, and emerging trends.
- Managing CTA submissions via CTIS for multiple EU member states, ensuring compliance with EU requirements.
- Organizing, preparing, and reviewing CTA amendments, annual reports, and other regulatory documents.
- Performing critical analyses of clinical and preclinical data to develop interpretations and conclusions.
- Leading EU Scientific Advice requests and coordinating EMA and EU national agency meetings.
- Monitoring newly published EU Commission and EMA guidelines to ensure compliance and provide training for scientific staff.
- Representing Regeneron Regulatory Affairs in engagements with EMA scientific committees, EU national agencies, and industry associations.
Qualifications
- Advanced degree in a scientific discipline.
- At least 4 years of regulatory experience, with a focus on clinical development.
- Proven experience supporting EU Clinical Trial Applications through approval and study start-up.
- Familiarity with EMA processes such as scientific advice, orphan designation, and PIPs.
- Experience in oncology regulatory strategy is an advantage.
- Strong ability to negotiate and express clear positions to stakeholders at all levels.
- Preferred qualifications include experience with marketing authorization applications or life-cycle management of approved products in the centralized procedure.
Why Join Us?
At Regeneron, we believe in fostering innovation, collaboration, and growth. You’ll have the opportunity to work with a passionate team dedicated to advancing science and improving patient outcomes. Together, we’ll make a difference.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels.
Equal Opportunity
Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company\’s business.
Additional Information
For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.
Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.
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Sr Mgr Regulatory Affairs employer: Regeneron
Contact Detail:
Regeneron Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Sr Mgr Regulatory Affairs
✨Network Like a Pro
Get out there and connect with people in the regulatory affairs field! Attend industry events, webinars, or even local meetups. Building relationships can open doors to opportunities that aren’t advertised.
✨Showcase Your Expertise
When you get the chance to chat with potential employers, don’t hold back on sharing your knowledge about EU regulations and oncology drug development. We want to see your passion and expertise shine through!
✨Prepare for Interviews
Research Regeneron and its recent projects in oncology. Be ready to discuss how your experience aligns with their goals. We love candidates who come prepared and show genuine interest in our mission.
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets noticed. Plus, it shows us you’re serious about joining our team at Regeneron.
We think you need these skills to ace Sr Mgr Regulatory Affairs
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Regulatory Affairs Manager role. Highlight your relevant experience in EU regulatory activities, especially in oncology, to show us you’re the perfect fit!
Showcase Your Expertise: Don’t hold back on detailing your regulatory experience! We want to see how you've managed CTA submissions and your familiarity with EMA processes. This is your chance to shine and demonstrate your knowledge.
Be Clear and Concise: When writing your application, keep it straightforward. Use clear language and avoid jargon where possible. We appreciate a well-structured application that gets straight to the point!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates from our team!
How to prepare for a job interview at Regeneron
✨Know Your Regulatory Stuff
Make sure you brush up on EU regulatory guidelines, especially those related to oncology. Familiarise yourself with the latest EMA processes and be ready to discuss how your experience aligns with their requirements.
✨Showcase Your Experience
Prepare specific examples from your past roles that highlight your regulatory experience, particularly with Clinical Trial Applications. Be ready to explain how you've navigated challenges and contributed to successful submissions.
✨Engage with the Interviewers
Don’t just answer questions; engage in a dialogue. Ask insightful questions about Regeneron’s current projects and how they align with your expertise. This shows your genuine interest and helps build rapport.
✨Stay Updated on Trends
Keep an eye on emerging trends in oncology and regulatory affairs. Being able to discuss recent developments or changes in guidelines will demonstrate your commitment to staying informed and proactive in your field.