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- Tasks: Lead exciting regulatory projects and guide teams to deliver high-quality results.
- Company: Join Veristat, a leader in accelerating life-changing therapies globally.
- Benefits: Flexible work culture, remote options, and a commitment to diversity.
- Why this job: Make a real impact in healthcare by supporting innovative therapies.
- Qualifications: 6-8 years in regulatory affairs with strong project management skills.
- Other info: Collaborative environment with opportunities for professional growth.
The predicted salary is between 36000 - 60000 £ per year.
The Senior Project Manager, Regulatory Affairs works as an integral part of the global Regulatory Affairs team to support the planning and execution of assigned Regulatory projects, guiding cross-functional teams to ensure delivery of high-quality deliverables within agreed timelines. The role collaborates internally with colleagues in Medical Writing, CMC and publishing teams, Medical, Quality and PV, business development, finance, other consulting functions, and regulatory leadership, and externally with sponsors, clients, vendors, and contractors.
To fulfil this role, the candidate should have a strong regulatory background, combined with experience in project management and project governance.
Make an Impact at Veristat! Veristat Global Regulatory team works across consulting and clinical trial programs from early development to approval and post-marketing, in close collaboration with the wider Veristat team.
- 105+ approved therapies for marketing applications prepared by Veristat
- 480+ oncology projects in the past 5 years
- 350+ rare disease projects delivered in the past 5 years
- Flexible, inclusive culture — 70% remote workforce, 66% women-led teams
What we look for:
- Bachelor’s degree in life/health sciences or related discipline, or equivalent required.
- 6 to 8 years of relevant Regulatory experience in a Clinical Research Organization or Pharmaceutical Company, with a minimum of 3 years of Project Management or functional team lead experience required.
- Excellent written and oral communication and interpersonal skills, as well as strong planning and organizational ability are required.
- Good working knowledge of Regulatory Affairs, Drug/Device development, including familiarity with applicable regulatory regulations and guidelines.
- Proficiency in English (written and verbal).
- Action-oriented and resilient in a fast-paced environment with the ability to build effective project teams, motivate others, delegate, and make and implement decisions.
- Ability to build and maintain trust and confidence and communicate effectively with clients, external vendors, and internal team members.
Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
Senior Project Manager, Regulatory Affairs in London employer: Veristat
Contact Detail:
Veristat Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Project Manager, Regulatory Affairs in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work in Regulatory Affairs. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Show us that you understand their mission and how your experience aligns with their goals. Tailor your answers to highlight your project management skills in a regulatory context.
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, drop a quick thank-you email to express your appreciation. It keeps you on their radar and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website for the best chance at landing that Senior Project Manager role. We love seeing candidates who take the initiative to engage directly with us!
We think you need these skills to ace Senior Project Manager, Regulatory Affairs in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Project Manager role. Highlight your regulatory experience and project management skills, and don’t forget to mention any relevant achievements that align with our values at StudySmarter.
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 makes you the perfect fit for our team. Keep it engaging and personal!
Showcase Your Communication Skills: Since excellent communication is key in this role, make sure your written application reflects that. Use clear, concise language and check for any typos or grammatical errors before hitting send.
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’re considered for the role. Plus, it shows you’re keen on joining the StudySmarter family!
How to prepare for a job interview at Veristat
✨Know Your Regulatory Stuff
Make sure you brush up on your knowledge of regulatory affairs and drug/device development. Be ready to discuss specific regulations and guidelines relevant to the role, as this will show that you’re not just familiar with the basics but can also navigate the complexities of the field.
✨Showcase Your Project Management Skills
Prepare examples from your past experiences where you successfully managed projects. Highlight your ability to lead cross-functional teams, meet deadlines, and deliver high-quality results. Use the STAR method (Situation, Task, Action, Result) to structure your responses.
✨Communicate Effectively
Since excellent communication is key for this role, practice articulating your thoughts clearly and concisely. Be prepared to demonstrate your interpersonal skills by engaging with the interviewers and asking insightful questions about the team and projects.
✨Emphasise Team Collaboration
This position involves working closely with various teams, so be ready to discuss how you’ve collaborated with different departments in the past. Share specific instances where you built trust and maintained effective communication with both internal and external stakeholders.
