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- Tasks: Lead pharmacovigilance activities and prepare safety reports for various projects.
- Company: Join a dynamic consultancy focused on patient safety and drug development.
- Benefits: Enjoy remote work, a 10% bonus, and private health insurance.
- Why this job: Be part of a collaborative team making a real impact in healthcare.
- Qualifications: 8-10 years in pharmacovigilance with strong regulatory knowledge required.
- Other info: Experience a streamlined interview process and diverse project opportunities.
The predicted salary is between 48000 - 72000 £ per year.
Chloe O'Shea is partnered with a Pharmacovigilance and Medical Consultancy that provides expert support across the drug development lifecycle, from early-phase clinical trials to post-marketing surveillance. Their client-centric model ensures agility and adaptability, allowing them to deliver high-quality pharmacovigilance solutions across all therapeutic areas, regulatory requirements, and product types. This consultancy thrives on collaboration, scientific precision, and a deep commitment to patient safety—supporting global clients with both strategic guidance and hands-on execution.
What we are looking for:
- A highly experienced Pharmacovigilance Scientist with 8–10 years’ industry experience, ideally across both clinical trial and post-marketing environments.
- Proven ability to manage a variety of therapeutic area (TA) projects—flexibility is key as this role supports multiple clients and drug types.
- A strong understanding of global pharmacovigilance regulations, risk management plans, aggregate report writing (PSURs, DSURs), and signal detection.
- Someone who thrives working autonomously but can collaborate effectively in remote, cross-functional teams.
- A proactive thinker with excellent attention to detail, strong writing skills, and a deep commitment to safety reporting excellence.
Main responsibilities:
- Lead end-to-end PV activities for assigned projects across clinical and post-marketing phases.
- Prepare, review, and finalize aggregate safety reports, risk management plans, and regulatory submissions in compliance with global standards.
- Perform signal detection, evaluation, and risk-benefit analysis, ensuring proactive safety monitoring across all client portfolios.
- Serve as a client-facing scientific expert, providing consultancy and strategic input on safety matters.
- Collaborate with internal teams and external partners to streamline PV operations, manage safety data, and respond to regulatory authority queries.
- Stay current with evolving regulations and industry trends, ensuring best practices are implemented and shared across teams.
What they offer:
- A fully remote, flexible working environment based in the UK.
- A 10% annual bonus, recognizing high performance and commitment.
- Private health insurance, supporting your well-being.
- A streamlined, one-stage interview process—efficient, focused, and candidate-friendly.
- The opportunity to work across diverse projects in a fast-moving, consultancy environment, where no two days are the same.
Senior Pharmacovigilance Scientist employer: AL Solutions
Contact Detail:
AL Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Pharmacovigilance Scientist
✨Tip Number 1
Familiarise yourself with the latest global pharmacovigilance regulations and guidelines. This knowledge will not only help you in interviews but also demonstrate your commitment to staying updated in a rapidly evolving field.
✨Tip Number 2
Network with professionals in the pharmacovigilance community, especially those who work in consultancy roles. Engaging with industry experts can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss specific projects you've managed in both clinical trial and post-marketing environments. Highlighting your flexibility and experience across various therapeutic areas will set you apart from other candidates.
✨Tip Number 4
Showcase your ability to work autonomously while also being an effective collaborator. Be ready to share examples of how you've successfully worked in remote teams, as this is crucial for the role.
We think you need these skills to ace Senior Pharmacovigilance Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your 8–10 years of experience in pharmacovigilance, particularly in both clinical trial and post-marketing environments. Emphasise your project management skills across various therapeutic areas.
Craft a Compelling Cover Letter: In your cover letter, demonstrate your understanding of global pharmacovigilance regulations and your experience with risk management plans and aggregate report writing. Use specific examples to showcase your attention to detail and proactive thinking.
Highlight Relevant Skills: Clearly outline your strong writing skills and ability to work autonomously while collaborating effectively in remote teams. Mention any experience you have with signal detection and safety reporting excellence.
Showcase Your Commitment to Patient Safety: In your application, express your deep commitment to patient safety and how it aligns with the consultancy's values. Discuss how you stay current with evolving regulations and industry trends to ensure best practices.
How to prepare for a job interview at AL Solutions
✨Showcase Your Experience
With 8–10 years of industry experience required, be ready to discuss specific projects you've managed. Highlight your roles in both clinical trials and post-marketing environments to demonstrate your versatility.
✨Understand Global Regulations
Familiarise yourself with global pharmacovigilance regulations and risk management plans. Be prepared to discuss how you have applied these in your previous roles, especially in relation to aggregate report writing and signal detection.
✨Emphasise Collaboration Skills
Since the role involves working in remote, cross-functional teams, share examples of how you've successfully collaborated with others. Highlight your ability to work autonomously while still being a team player.
✨Demonstrate Attention to Detail
Given the importance of safety reporting excellence, prepare to discuss how you ensure accuracy in your work. Bring examples of how your attention to detail has positively impacted your previous projects.
