Senior Pharmacovigilance Project Manager- Europe

ppbCompany Description /b Medicine moves forward here. So will you. /p /brpbCompany Description /b Medicine moves forward here. So will you. /p /brpAt PrimeVigilance, patient safety is not one part of the job. It is why we exist. /p /brpWe 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. /p /brpThat 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. /p /brpIf 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. /p /brpbJob Description /b /p /brul /brliActing as the primary contact point for project-related matters /li /brliManaging client’s expectations to make sure the client is satisfied with services of PrimeVigilance, and that the work PrimeVigilance delivers meets, or even exceeds, the clients’ expectations. /li /brliPreparing project scope and objectives based on the signed agreement between the client and PrimeVigilance. /li /brliProject activities planning, including deadlines and interim milestones /li /brliReporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing. /li /br /ul /brpbQualifications /b /p /brul /brliProven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSS, writing, or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs /li /brliPV Project Management experience from ideally a service provide / CRO /li /brliHealth Care Professional or Life Science Graduate /li /brliBe comfortable with communicating at senior levels within pharmaceutical organizations /li /brliHave good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving. /li /br /ul /brpbAdditional Information /b 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. /p /brpWe 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. /p /brul /brliQuality: we hold ourselves to the standard patients deserve. /li /brliIntegrity and trust: we do the right thing, especially when it is hard. /li /brliDrive and passion: we care about the outcome, because someone is waiting on it. /li /brliAgility and responsiveness: we move quickly, because patients cannot wait. /li /brliBelonging: everyone is welcome, and every voice counts. /li /brliCollaborative partnerships: we go further by going together. /li /br /ul /brpWe look forward to welcoming your application. /p /p #J-18808-Ljbffr