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- Tasks: Lead pharmacovigilance activities and prepare safety reports for diverse projects.
- Company: Join a dynamic consultancy focused on patient safety and drug development.
- Benefits: Enjoy remote work, a 10% annual bonus, and private health insurance.
- Why this job: Be part of a collaborative team making a real impact in healthcare.
- Qualifications: 8-10 years of experience in pharmacovigilance with strong writing skills.
- Other info: Experience a streamlined interview process and a flexible working environment.
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 in discussions on platforms like LinkedIn can provide insights into the industry and may even lead to referrals.
✨Tip Number 3
Prepare to discuss specific therapeutic area projects you've managed in the past. Highlighting your flexibility and ability to handle multiple clients will resonate well with the consultancy's client-centric model.
✨Tip Number 4
Showcase your experience with risk management plans and aggregate report writing during conversations. Being able to articulate your hands-on experience in these areas will set you apart as a strong candidate for this 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 Safety: Express your deep commitment to patient safety and how you stay current with evolving regulations and industry trends. This will resonate well with the consultancy's focus on safety and high-quality pharmacovigilance solutions.
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 Proactive Thinking
The consultancy values proactive thinkers. Prepare to discuss instances where you've identified potential safety issues or improved processes. Show your commitment to patient safety and excellence in safety reporting.
