Senior Pharmacovigilance Scientist

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

Job summary

A forward-thinking consultancy is seeking a Clinical Operations Specialist with extensive experience in pharmacovigilance. This fully remote role offers the chance to lead critical safety activities across diverse projects in a dynamic environment. You will be responsible for ensuring compliance with global regulations while providing expert consultancy to clients. With a focus on collaboration and scientific precision, this position is ideal for proactive individuals who thrive in a fast-paced setting. Join a team that values your expertise and offers a competitive bonus structure, all while working from the comfort of your home.

Benefits

10% annual bonus

Fully remote working environment

Streamlined interview process

Diverse project opportunities

Qualifications

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

Responsibilities

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

Skills

Pharmacovigilance

Regulatory Compliance

Risk Management

Signal Detection

Attention to Detail

Writing Skills

Education

Bachelor's Degree in Life Sciences

Advanced Degree (e.g., MSc, PhD)

Job description

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Clinical Operations Specialist at AL Solutions

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.

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Research

• Industries

  Pharmaceutical Manufacturing and Biotechnology Research

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