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- Tasks: Provide expert regulatory consulting and lead complex projects in a collaborative environment.
- Company: Join an award-winning CRO known for its supportive culture and employee satisfaction.
- Benefits: Enjoy a flexible remote work setup and opportunities for professional growth.
- Why this job: Make a real impact in the pharmaceutical and biotech industries while advancing your career.
- Qualifications: 15+ years in regulatory consulting with strong communication and problem-solving skills.
- Other info: Be part of a dynamic team shaping the future of clinical research.
The predicted salary is between 36000 - 60000 £ per year.
Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is an award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognised for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career.
Principal Regulatory Strategist Responsibilities- Provide consulting and advisory services for complex regulatory issues or projects.
- Author and maintain documentation as required to sustain regulatory compliance.
- Provide senior technical review for complex regulatory projects.
- Conduct regulatory intelligence gathering to support development of regulatory roadmaps, complex feasibility assessments, and other regulatory intelligence reports.
- Participate on project teams and provide expertise on related regulatory matters.
- Clearly and accurately convey information to peers, supervisors, and other stakeholders.
- Participate in implementation of new/updated operational strategies to comply with new/updated policies and recommendations.
- Identify new/updated policies and recommendations and may provide professional opinions on impact of regulatory changes to MMS and Clients.
- Provide internal and cross-functional leadership and contribute to the development of robust processes and procedures when needed.
- College graduate in Biological Science, Public Health, or Regulatory Science or related field, or related experience, Masters or PhD preferred.
- Minimum of 15 years' experience in Regulatory Consulting (Affairs or Strategy) or similar field required, including experience with Marketing Applications (EMA).
- Expert knowledge of regulatory principles and concepts.
- Reputation as emerging leader in field with sustained performance and accomplishment.
- Proficiency with MS Office applications.
- Hands-on experience with clinical trial and pharmaceutical development preferred.
- Expert communication skills and willingness to work with others to clearly understand needs and solve problems.
- Excellent problem-solving skills.
- Good organisational and communication skills.
- Basic understanding of CRO-based consulting and scientific and clinical data/terminology, and the drug development process.
Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.
Principal Regulatory Strategist (CRO Industry) - Europe, Remote Regulatory Affairs - Regulatory[...] in London employer: MMS Holdings Inc
Contact Detail:
MMS Holdings Inc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Principal Regulatory Strategist (CRO Industry) - Europe, Remote Regulatory Affairs - Regulatory[...] in London
✨Network Like a Pro
Get out there and connect with people in the CRO industry! Attend webinars, join LinkedIn groups, and don’t be shy about reaching out to current employees at MMS. A friendly chat can sometimes lead to opportunities that aren’t even advertised!
✨Show Off Your Expertise
When you get the chance to speak with someone from MMS, make sure to highlight your experience in regulatory consulting. Share specific examples of how you've tackled complex regulatory issues. This will show them you’re not just another candidate, but someone who can truly contribute to their innovative team.
✨Prepare for the Interview
Do your homework on MMS and the role of Principal Regulatory Strategist. Understand their projects and challenges in the CRO space. Prepare thoughtful questions that demonstrate your knowledge and enthusiasm for the position. This will set you apart from the crowd!
✨Apply Through Our Website
Don’t forget to apply directly through the MMS website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in being part of their amazing team.
We think you need these skills to ace Principal Regulatory Strategist (CRO Industry) - Europe, Remote Regulatory Affairs - Regulatory[...] in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the specific skills and experiences that match the Principal Regulatory Strategist role. Highlight your expertise in regulatory consulting and any relevant projects you've worked on, as this will show us you're a great fit for our team.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you're passionate about regulatory affairs and how your background aligns with our mission at MMS. Be genuine and let your personality come through!
Showcase Your Communication Skills: Since communication is key in this role, make sure your application materials are clear and concise. We want to see how you convey complex information effectively, so pay attention to your writing style and structure.
Apply Through Our Website: We encourage you to apply directly through our website. This not only streamlines the process but also ensures your application gets the attention it deserves. Plus, you'll find more info about our culture and values there!
How to prepare for a job interview at MMS Holdings Inc
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of regulatory principles and concepts. Given the role's focus on complex regulatory issues, being able to discuss specific examples from your past experience will show that you’re not just familiar with the theory but can apply it in practice.
✨Showcase Your Leadership Skills
As a Principal Regulatory Strategist, you'll need to demonstrate your ability to lead and influence others. Prepare examples of how you've provided internal leadership or contributed to cross-functional teams in previous roles. This will highlight your collaborative spirit and problem-solving skills.
✨Communicate Clearly
Excellent communication is key in this role. Practice articulating complex regulatory concepts in a straightforward manner. You might even want to prepare a few scenarios where you had to convey important information to stakeholders, showcasing your ability to simplify complex topics.
✨Stay Updated on Industry Changes
Regulatory affairs are constantly evolving, so it’s crucial to stay informed about the latest policies and recommendations. Be ready to discuss recent changes in the industry and how they could impact MMS and its clients. This shows your proactive approach and genuine interest in the field.
