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- Tasks: Lead exciting regulatory projects and guide teams to deliver high-quality results.
- Company: Join Veristat, a global leader in regulatory affairs with over 30 years of expertise.
- Benefits: Enjoy a flexible, inclusive culture with remote work options and diverse teams.
- Why this job: Make a real impact on life-changing therapies and collaborate with top professionals.
- Qualifications: 6-8 years in regulatory affairs and project management; strong communication skills required.
- Other info: Be part of a dynamic team dedicated to accelerating patient access to therapies.
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.
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 employer: Veristat
Contact Detail:
Veristat Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Project Manager, Regulatory Affairs
✨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 you’re genuinely interested in Veristat and how your experience aligns with their mission. Tailor your answers to highlight your regulatory expertise!
✨Tip Number 3
Practice your communication skills! As a Senior Project Manager, you’ll need to convey complex information clearly. Try mock interviews with friends or use online platforms to refine your pitch.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the Veristat team!
We think you need these skills to ace Senior Project Manager, Regulatory Affairs
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, using keywords from the job description to catch our eye!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Share your passion for regulatory affairs and how your background aligns with our mission at Veristat. Keep it concise but impactful!
Showcase Your Communication Skills: Since excellent communication is key for this role, ensure your application reflects your written communication skills. Use clear language and structure to demonstrate your ability to convey complex information effectively.
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 our team!
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 in a two-way conversation during the interview, showing that you can build trust and rapport with clients and team members.
✨Embrace the Company Culture
Familiarise yourself with Veristat’s core values and their inclusive culture. During the interview, express how your personal values align with theirs and share any experiences that reflect your adaptability and resilience in fast-paced environments. This will help you stand out as a candidate who fits well within their team.
