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- Tasks: Lead business analysis for regulatory intelligence in healthcare, translating complex requirements into actionable solutions.
- Company: 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 healthcare by driving compliance and innovation.
- 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 Plymouth 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 Plymouth
✨Tip Number 1
Network like a pro! Reach out to your connections in the healthcare and life sciences sectors. Attend virtual meetups or webinars to get your name out there and show off your expertise in regulatory affairs.
✨Tip Number 2
Prepare for those interviews by brushing up on Agile methodologies and regulatory compliance. We recommend practising common interview questions related to business analysis and having examples ready that showcase your experience in translating complex requirements.
✨Tip Number 3
Don’t just apply anywhere; focus on roles that excite you! Use our website to find positions that match your skills and interests, especially those involving regulatory intelligence platforms and automation.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in keeping you top of mind. Mention something specific from your conversation to show you were engaged and are genuinely interested in the role.
We think you need these skills to ace Regulatory Business Analyst – Healthcare/Life Sciences - £400 (Outside IR35) – Remote in Plymouth
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, and don’t forget to mention any Agile methodologies you’ve used. 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. We love a good story!
Showcase Your Communication Skills: Since this role involves managing stakeholders at all levels, make sure your application reflects your excellent communication skills. Whether it’s through your CV, cover letter, or any additional documents, let us see how you can convey complex information clearly and 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 don’t miss out on any important updates. Plus, it shows us you’re keen to join our team!
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 Agile delivery, be prepared to talk about your experience with user story writing and how you've used Agile methodologies in past projects. Bring examples of how you’ve translated complex requirements into actionable tasks for teams.
✨Show Off Your Process Mapping Skills
Have a few examples ready that demonstrate your process mapping and documentation skills. Discuss how you’ve improved processes in previous roles, especially in a life sciences or pharmaceutical context, to highlight your analytical abilities.
✨Communicate Like a Pro
Excellent communication is key in this role, so practice articulating your thoughts clearly and confidently. Be ready to explain how you’ve managed stakeholders at various levels and how you ensure everyone is aligned during projects.