Sr. Medical Information Assistant/Medical Information Assistant

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 Assistant to be responsible for supporting the Medical Information team in handling various administrative duties.   Responsibilities  Administration support for meetings, invoice activities, generating reports  Maintenance of Medical Information systems and department documentation  Engagement in pharmacovigilance and quality complaint follow-up activities  Administrative support with Medical Information Enquiries, Adverse Event and Product Quality  Complaint Activities  Administrative support in new client onboarding activities  To assist in departmental regulatory inspection preparedness for the company  Advanced English skills, both verbal and written, at least B2   Desirable administrative experience and good IT skills (MS Office)   A high degree of discretion dealing with confidential information   Ability to manage multiple and varied tasks and prioritize workload with attention to detail   Ability to work under pressure with accuracy and meet tight deadlines   Good interpersonal and communication skills  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.