Senior Pharmacovigilance Scientist

JR United Kingdom; United Kingdom; Remote; GBP 50,000 - 80,000; Full time

Job summary

An innovative consultancy seeks a highly experienced Pharmacovigilance Scientist to lead end-to-end activities across diverse projects in a fully remote environment. With a commitment to patient safety and regulatory excellence, this role offers the chance to collaborate with global clients and internal teams, ensuring proactive safety monitoring and strategic consultancy. Enjoy a flexible working atmosphere, a competitive annual bonus, and a streamlined interview process that prioritizes candidate experience. If you're a proactive thinker with a passion for pharmacovigilance, this opportunity is perfect for you.

Benefits

Fully remote working environment

10% annual bonus

One-stage interview process

Diverse project opportunities

Qualifications

• 8-10 years of experience in pharmacovigilance, especially in clinical and post-marketing.
• Strong understanding of global pharmacovigilance regulations and risk management.

Responsibilities

• Lead end-to-end pharmacovigilance activities for clinical and post-marketing projects.
• Prepare and finalize aggregate safety reports and regulatory submissions.

Skills

Pharmacovigilance

Signal Detection

Risk Management

Attention to Detail

Writing Skills

Job description

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Client:

AL Solutions

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Other

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EU work permit required:

Yes

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Job Views:

3

Posted:

05.05.2025

Expiry Date:

19.06.2025

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Job Description:

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.
• 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.