Senior Pharmacovigilance Associate
Ergomed
Senior Pharmacovigilance Associate
Ergomed
Runs clinical trials and monitors drug safety
When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.
Quality: we hold ourselves to the standard patients deserve.
Integrity and trust: we do the right thing, especially when it is hard.
Drive and passion: we care about the outcome, because someone is waiting on it.
Agility and responsiveness: we move quickly, because patients cannot wait.
Belonging: everyone is welcome, and every voice counts.
Collaborative partnerships: we go further by going together.
We look forward to welcoming your application.
Ergomed manages clinical trials and drug safety for biotechnology and pharmaceutical companies, with a focus on complex cancer and rare-disease studies. Its clinical research business supports development from early testing through studies after approval, with services adapted to difficult patient populations. Teams plan trials, recruit patients, monitor study sites, and analyze results under paid service contracts. PrimeVigilance tracks medicine safety and answers medical inquiries, while ADAMAS Consulting advises clients on quality and regulatory compliance across drug development. Ergomed was founded in 1997 and has its global headquarters in Guildford, Surrey, United Kingdom.
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