At a Glance
- Tasks: Lead global regulatory submissions and coordinate cross-functional teams for high-quality outcomes.
- Company: Join UCB, a global biopharmaceutical company focused on neurology and immunology.
- Benefits: Enjoy a supportive culture, hybrid work, and opportunities for personal growth.
- Other info: Collaborative atmosphere where innovation and inclusion are at the forefront.
- Why this job: Make a real impact for patients while developing your career in a dynamic environment.
- Qualifications: Degree in science or related field with 5+ years in pharmaceuticals or regulated environments.
The predicted salary is between 70000 - 90000 £ per year.
Make your mark for patients. We are looking for a Global Submission Lead who is collaborative, organised, and solution-focused to join our Regulatory Community Excellence & Operations team, based in either of our Brussels (Belgium), Slough (UK) or Atlanta/Raleigh (US) offices.
About the role: You will shape and drive global regulatory submissions from strategic planning through execution. You will coordinate cross-functional teams, keep submission plans on track, manage risks and priorities, and help stakeholders stay aligned. You will bring structure, clear communication, and practical problem-solving to complex submission activities so teams can deliver high-quality outcomes on agreed timelines.
Who you will work with: You will work with sponsors, regulatory colleagues, project teams, and internal and external stakeholders across multiple areas of expertise. You will create a safe, collaborative environment where people can share information, make decisions, and move towards common goals. You will also support colleagues by sharing lessons learned and helping others build project management capability.
What you will do: You will initiate and guide strategic submission plans that support global regulatory objectives and agreed timelines. You will lead cross-functional submission teams, helping people stay aligned, informed, and focused on priorities. You will identify risks, issues, and changing priorities early, then work with stakeholders to agree practical solutions. You will manage meetings, agendas, minutes, follow-ups, and project tools such as SharePoint and planning systems. You will develop clear communications and reports for internal and external stakeholders to support effective decision-making. You will contribute to better ways of working by sharing lessons learned, challenges, solutions, and best practices.
Interested? For this role, we are looking for the following education, experience, and skills: You have a degree in science, engineering, health, or a related field; advanced qualifications are welcome. You bring over five years of experience in pharmaceuticals, CROs, drug development, or a comparable regulated environment. You understand regulatory processes, Common Technical Document requirements, drug development, and submission procedures. You have strong project management skills and can manage uncertainty, risk, priorities, and timelines effectively. You communicate clearly in English and can facilitate, influence, negotiate with diverse stakeholders. You are comfortable working independently and collaboratively, with strong problem-solving, adaptability, cultural awareness, and attention to detail.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us: UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are over 9,000 people in all four corners of the globe, inspired by patients and driven by science.
Why work with us? At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected, and has equal opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees, or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential. At UCB, we’ve embraced a hybrid‑first approach to work, bringing teams together in local hubs to foster collaborative curiosity. Unless expressly stated in the description or precluded by the nature of the position, roles are hybrid with 40% of your time spent in the office. UCB is an equal opportunity employer. All employment decisions will be made without regard to any characteristic protected by applicable laws. Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on EMEA-Reasonable_Accommodation@ucb.com. Please note should your enquiry not relate to adjustments; we will not be able to support you through this channel.
Global Submission Lead Slough employer: Meeveem Limited
UCB is an exceptional employer that prioritises collaboration, innovation, and employee growth within a supportive culture. Based in Slough, you will be part of a global biopharmaceutical team dedicated to making a meaningful impact on patients' lives, with opportunities for professional development and a hybrid work model that fosters teamwork and flexibility. Join us to thrive in an environment where your contributions are valued and you can truly make your mark.
StudySmarter Expert Advice🤫
We think this is how you could land Global Submission Lead Slough
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We think you need these skills to ace Global Submission Lead Slough
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Meeveem Limited!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Meeveem Limited that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at Meeveem Limited!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At Meeveem Limited, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at Meeveem Limited
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Meeveem Limited that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
Take some time to familiarise yourself with Meeveem Limited’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.
✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
