Location: Remote (within the EU or UK)
Type: Full-time | Freelance/Contract Options Available
Join a Global Leader in Drug Safety as a Remote Pharmacovigilance Scientist (EU/UK)
We are currently partnering with a global pharmacovigilance services and technology provider to recruit a Pharmacovigilance Scientist based in the EU or UK. This is a fully remote opportunity to join a growing safety science team and contribute to the evaluation and oversight of pharmaceutical product safety worldwide.
The company is widely recognized for its smart, scalable PV solutions—supporting regulatory compliance, benefit-risk evaluation, and post-marketing safety across all phases of the product lifecycle.
Responsibilities – What You’ll Do
As a Pharmacovigilance Scientist (EU Remote), you’ll collaborate with Safety Physicians and Global Safety Officers on a range of safety and regulatory projects:
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Perform benefit-risk evaluations and support safety decisions across global programs
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Evaluate adverse events (AEs) and trends in clinical and post-marketing data
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Draft and review safety narratives, case summaries, and regulatory submission content
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Contribute to safety signal detection and signal management activities
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Prepare high-quality regulatory documents, including PSURs, PBRERs, DSURs, and RMPs
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Participate in inspection readiness, SOP/WI development, and process improvement
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Stay current with evolving global PV regulations (EMA, MHRA, FDA, etc.)
Ideal Candidate Profile
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Bachelor’s, Master’s, or Doctoral degree in life sciences, pharmacy, medicine, or related field
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3–5 years of hands-on PV experience, particularly in safety science or risk management
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Familiarity with AE/SAE processing, MedDRA coding, and global clinical trial standards
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Experience preparing safety deliverables for regulatory agencies
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Strong analytical, writing, and interpersonal communication skills
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Excellent attention to detail and ability to work independently
Preferred Skills
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Experience using safety databases (e.g., Argus, ArisG, Veeva Vault Safety)
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Fluent in English; other European languages are an advantage
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Proficient in Microsoft Office Suite (Excel, Word, PowerPoint)
Why Apply?
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Join a respected industry leader in pharmacovigilance outsourcing and technology
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Work fully remote from anywhere in the EU or UK
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Flexible contract or full-time engagement available
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Contribute to patient safety and global public health through impactful work
Apply Now
If you’re a Pharmacovigilance Scientist based in the EU/UK looking to expand your impact with a dynamic, tech-enabled safety science team, we want to hear from you.
📧 Send your CV to Daniel Bishop at: Daniel@greenlsr.com
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