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- Tasks: Lead regulatory strategy and submissions for BMS UK/Ireland portfolio.
- Company: Bristol Myers Squibb, a leader in life-changing science.
- Benefits: Competitive benefits, flexible work environment, and career growth opportunities.
- Why this job: Transform lives through science while advancing your career in a supportive culture.
- Qualifications: Degree in life sciences and 6+ years in regulatory leadership.
- Other info: Join a diverse team committed to innovation and inclusion.
The predicted salary is between 48000 - 72000 £ per year.
Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible. Bristol Myers Squibb recognises the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.
Role Summary Lead and execute the regulatory strategy for BMS UK/Ireland portfolio, driving submissions, health authority interactions, and team development in alignment with commercial and R&D objectives.
Key Responsibilities
- Regulatory Strategy & Submissions
- Own end-to-end regulatory strategy for assigned UK/Ireland portfolio
- Drive marketing authorisation applications, line extensions, lifecycle management, and clinical trial applications (CTAs)
- Ensure timely product registrations
- Maintain approved labelling in line with local legislation
- Health Authority Engagement
- Serve as primary liaison with MHRA, HPRA, and DHSC
- Develop external networks with Health Authorities and Trade Associations
- Cross-functional Partnership
- Collaborate with Medical, PV, Market Access, Commercial, GMS, and Global/EU GRS teams
- Provide regulatory input for pipeline compounds and pre-/launch activities
- Lead Quality & Compliance for GRS UK/Ireland
- People Leadership
- Lead, coach, and develop a high-performing, diverse UK/Ireland GRS team
- Foster a culture of inclusion, accountability, and continuous improvement
Qualifications
- Education: Degree in life sciences (MSc/PhD preferred)
- Experience: 6+ years in country regulatory leadership (UK/Ireland preferred)
- Skills: Strategic regulatory planning, people management, health authority engagement, cross-functional collaboration, RIM systems proficiency
- Travel: Minimal
If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as "Transforming patients’ lives through science™", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
Associate Director, Global Regulatory Sciences (GRS) Lead, UK&IE in London employer: Bristol-Myers Squibb
Contact Detail:
Bristol-Myers Squibb Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Associate Director, Global Regulatory Sciences (GRS) Lead, UK&IE in London
✨Tip Number 1
Network like a pro! Reach out to current or former employees at Bristol Myers Squibb on LinkedIn. A friendly chat can give you insider info and maybe even a referral, which can really boost your chances.
✨Tip Number 2
Prepare for the interview by knowing your stuff! Research BMS’s recent projects and their impact on patients. This shows you're genuinely interested and ready to contribute to their mission of transforming lives.
✨Tip Number 3
Practice makes perfect! Get a friend to do mock interviews with you. Focus on articulating your experience in regulatory strategy and how it aligns with BMS’s goals. Confidence is key!
✨Tip Number 4
Don’t hesitate to apply through our website! Even if you think you don’t tick every box, go for it. You might just be the candidate they didn’t know they were looking for!
We think you need these skills to ace Associate Director, Global Regulatory Sciences (GRS) Lead, UK&IE in London
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter to highlight how your experience aligns with the role. We want to see how you can contribute to our mission of transforming patients' lives through science!
Showcase Your Leadership Skills: As an Associate Director, you'll be leading a team, so don’t forget to emphasise your people management experience. Share examples of how you've developed high-performing teams in the past.
Highlight Regulatory Expertise: Since this role involves regulatory strategy and health authority engagement, make sure to detail your experience in these areas. We’re looking for someone who knows their stuff when it comes to submissions and compliance!
Apply Through Our Website: We encourage you to apply directly through our careers page. It’s the best way to ensure your application gets the attention it deserves. Plus, you’ll find all the info you need about the role there!
How to prepare for a job interview at Bristol-Myers Squibb
✨Know Your Regulatory Stuff
Make sure you brush up on the latest regulations and guidelines relevant to the UK and Ireland. Familiarise yourself with the MHRA and HPRA processes, as well as any recent changes in legislation that could impact your role. This will show your potential employer that you're not just knowledgeable but also proactive about staying updated.
✨Showcase Your Leadership Skills
As an Associate Director, you'll be expected to lead a team. Prepare examples of how you've successfully managed teams in the past, focusing on fostering inclusion and accountability. Think about specific challenges you've faced and how you overcame them while developing your team's capabilities.
✨Engage with Cross-Functional Teams
Collaboration is key in this role. Be ready to discuss your experience working with various departments like Medical, Market Access, and Commercial. Highlight instances where your regulatory input made a significant impact on project outcomes, demonstrating your ability to work effectively across functions.
✨Prepare Questions for Them
Interviews are a two-way street! Prepare thoughtful questions about their regulatory strategy and how they envision the role evolving. This not only shows your interest in the position but also gives you insight into whether the company culture aligns with your values and career goals.