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- Tasks: Lead business analysis for regulatory intelligence in healthcare, translating complex requirements into actionable solutions.
- Company: Join a leading healthcare client focused on compliance and efficiency.
- Benefits: £400 daily rate, remote work, and potential for contract extension.
- Why this job: Make a real impact in the healthcare sector while working with cutting-edge regulatory technology.
- Qualifications: Experience in business analysis within life sciences and understanding of global regulatory standards.
- Other info: Initial 2-month contract with opportunities for travel to London office.
Leading Healthcare client now requires an experienced Regulatory Business Analyst to lead business analysis activities across their regulatory intelligence programme. You will sit at the intersection of regulatory affairs, technology, and operations — translating complex regulatory requirements into actionable solutions that drive compliance and efficiency across a global business.
What you will do:
- Lead requirements gathering and documentation with regulatory affairs and operations stakeholders.
- Translate regulatory requirements into user stories, functional specs, and process workflows using Agile methodologies.
- Support the full regulatory intelligence lifecycle — from capture and curation through to consumption.
- Drive implementation of regulatory intelligence platforms and SaaS solutions, including UAT and validation.
- Analyse global regulatory updates and perform gap analysis to define improved future-state processes.
- Work across eCTD submissions, labeling updates, and CMC variation processes.
What we are looking for:
- Strong Business Analysis experience within a life sciences or pharmaceutical environment.
- Solid understanding of global regulatory standards and compliance requirements.
- Hands-on experience with Agile delivery, user story writing, and cross-functional stakeholder management.
- Excellent process mapping and documentation skills.
- Familiarity with regulatory intelligence platforms and a keen interest in automation and AI-driven solutions.
- Excellent communication skills with the ability to manage stakeholders of all levels.
This is an initial 2-month contract role (rolling) which provides a daily rate of £400 Outside IR35. In terms of working structure, this is remote with occasional travel to our client's London office.
Regulatory Business Analyst – Healthcare/Life Sciences - £400 (Outside IR35) – Remote in Coventry employer: Ventula Consulting
Contact Detail:
Ventula Consulting Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Business Analyst – Healthcare/Life Sciences - £400 (Outside IR35) – Remote in Coventry
✨Tip Number 1
Network like a pro! Reach out to your connections in the healthcare and life sciences sectors. A quick chat can lead to opportunities that aren’t even advertised yet.
✨Tip Number 2
Prepare for those interviews by brushing up on your Agile methodologies and regulatory knowledge. We want you to be able to showcase how you can translate complex requirements into actionable solutions.
✨Tip Number 3
Don’t forget to tailor your approach! When you’re discussing your experience, highlight your hands-on work with regulatory intelligence platforms and your knack for stakeholder management.
✨Tip Number 4
Finally, apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Regulatory Business Analyst – Healthcare/Life Sciences - £400 (Outside IR35) – Remote in Coventry
Some tips for your application 🫡
Tailor Your CV: Make sure your CV speaks directly to the job description. Highlight your experience in regulatory affairs and business analysis, especially within life sciences. We want to see how your skills align with what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're the perfect fit for this role. Share specific examples of how you've translated complex regulatory requirements into actionable solutions in the past.
Showcase Your Agile Experience: Since we’re keen on Agile methodologies, make sure to mention any hands-on experience you have with user story writing and cross-functional stakeholder management. We love seeing how you’ve driven projects forward in a collaborative environment!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. We can’t wait to see what you bring to the table!
How to prepare for a job interview at Ventula Consulting
✨Know Your Regulatory Stuff
Make sure you brush up on global regulatory standards and compliance requirements before the interview. Being able to discuss specific regulations and how they impact business operations will show that you’re not just familiar with the theory, but you can apply it practically.
✨Master Agile Methodologies
Since the role involves translating regulatory requirements into user stories and functional specs using Agile, be prepared to discuss your experience with Agile delivery. Bring examples of how you've successfully implemented Agile practices in past projects, especially in a life sciences context.
✨Show Off Your Communication Skills
This position requires excellent communication skills for managing stakeholders at all levels. Think of examples where you’ve effectively communicated complex information to diverse audiences. Practise articulating these experiences clearly and confidently.
✨Prepare for Process Mapping Questions
Given the emphasis on process mapping and documentation, be ready to discuss your approach to these tasks. Have a couple of examples handy that demonstrate your ability to analyse processes and suggest improvements, particularly in relation to regulatory intelligence.