Medical Information Associate

Medicine moves forward here. So will you.  At PrimeVigilance, patient safety is not one part of the job. It is why we exist.  We are a global pharmacovigilance specialist. Our teams help clients navigate complex regulations while keeping patient safety at the center of every decision, from early development through to post-marketing surveillance. Increasingly, the value we create is not only in processing safety data but in interpreting it: spotting the signal that matters early and turning it into insight our clients can act on.  That work takes curious minds, problem-solvers and experts who care about getting it right. It also takes a culture worth staying for. Across Europe, North America, South America, Asia and Australia, we work in an environment built on kindness, flexibility, growth and belonging, where colleagues support one another and good ideas are heard wherever they come from.  If you want a role with real purpose, global reach and the chance to keep growing while you help protect patients, you will feel at home here. We would love to hear from you. PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries .    Responsibilities  • To provide approved responses to medical enquiries (healthcare professionals, patients, pharmaceutical clients) including call handling   • To accurately identify, document and report adverse events/side effects, pregnancy and other special situation events, and product quality complaints within required timeframes  • To ensure that all medical information enquiries are tracked and fully documented within the Medical Information database accurately and completely  • To participate in the out-of-hours provision of medical information for clients who have contracted a 24/7 enquiry handling service   • Providing management with regular updates regarding project status and metrics concerning enquiries  • Assisting in departmental regulatory inspection preparedness for the company pharmacovigilance system and actively participating in PV inspections or audits;   Life science / bio medical background – healthcare related degree (chemistry, biology, biotechnology, pharmacy, nursing)  Fluency in English, additional language skills in Mandarin, Cantonese, Thai or Korean preferred. 0-3 years of work experience in medical information or pharmacovigilance Customer service or call centre experience preferred  Comfortable receiving enquires by phone Ability to perform out-of-hours service if required  Time and issue management, delegation, organization and multitasking skills with good attention to detail  Strong interpersonal and communication skills  comfortable reading and writing in English. 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.