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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
Network with professionals in the pharmacovigilance field. Attend industry conferences, webinars, or local meetups to connect with others who work in similar roles. This can help you gain insights into the company culture and potentially get a referral.
✨Tip Number 2
Familiarise yourself with the latest global pharmacovigilance regulations and trends. Being well-versed in current guidelines will not only boost your confidence but also demonstrate your commitment to safety reporting excellence during discussions.
✨Tip Number 3
Prepare to discuss specific therapeutic area projects you've managed in the past. Highlight your flexibility and ability to handle multiple clients and drug types, as this is crucial for the role. Real-life examples will make your experience more relatable.
✨Tip Number 4
Showcase your collaborative skills by discussing experiences where you've worked in remote, cross-functional teams. Emphasising your ability to thrive autonomously while still being a team player will resonate well with the consultancy's values.
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 in both clinical trial and post-marketing environments. Highlight your flexibility in handling various therapeutic areas and how you've adapted to different client needs.
✨Demonstrate Regulatory Knowledge
Make sure to brush up on global pharmacovigilance regulations and risk management plans. Be prepared to discuss your experience with aggregate report writing, such as PSURs and DSURs, and how you approach signal detection.
✨Emphasise Collaboration Skills
Even though the role requires autonomy, collaboration is key. Share examples of how you've successfully worked in remote, cross-functional teams, and how you’ve contributed to streamlining operations and managing safety data.
✨Highlight Attention to Detail
Given the importance of safety reporting excellence, be ready to provide examples that showcase your attention to detail. Discuss how this skill has positively impacted your previous work and contributed to patient safety.
