助理药物警戒项目经理（欧洲）
Associate Pharmacovigilance Project Manager (Europe)
医学在这里不断前进，你也将随之成长。
在PrimeVigilance，患者安全不是工作的某一部分，而是我们存在的理由。
我们是一家全球药物流行病学专家。我们的团队帮助客户应对复杂的法规，同时将患者安全置于每个决策的核心，从早期开发到上市后监测。越来越多地，我们创造的价值不仅在于处理安全数据，还在于解读数据：尽早发现重要的信号，并将其转化为客户可以采取行动的见解。
这项工作需要充满好奇心的头脑、解决问题的人才以及关心把事情做对的专家。它还需要一个值得留下的文化。在欧洲、北美、南美、亚洲和澳大利亚，我们在一个以善良、灵活性、成长和归属感为基础的环境中工作，同事之间互相支持，无论来自何处的好想法都会被听到。
如果你想要一份有真正意义、具有全球影响力，并且在帮助保护患者的同时能够持续成长的工作，你会在这里感到如鱼得水。我们期待收到你的来信。
- 作为项目相关事务的主要联系人
- 管理客户期望，确保客户对PrimeVigilance的服务满意，并且PrimeVigilance交付的工作满足甚至超越客户的期望。
- 根据客户与PrimeVigilance签署的协议，制定项目范围和目标。
- 项目活动计划，包括截止日期和中间里程碑
- 向客户和PrimeVigilance管理层报告，例如编制月度报告，作为开票的基础。
- 具有药物流行病学活动的显著业绩，包括处理和质量审查ICSRs、撰写或参与汇总报告、文献筛选、核对以及SOP的准备
- 具备药物流行病学项目管理经验，最好是来自服务提供商/CRO
- 医疗保健专业人员或生命科学专业毕业生
- 能够在制药组织中与高级别人员进行沟通
- 具备良好的领导素质，包括规划、指导、会议主持、沟通和解决问题的能力
当你加入Ergomed集团时，你将通过帮助为全球患者带来安全有效的药物治疗而产生影响。你将加入一个充满热情和协作精神的专家团队，专注于临床研究、药物流行病学、
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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.
- Acting as the primary contact point for project-related matters
- Managing 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.
- Preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance.
- Project activities planning, including deadlines and interim milestones
- Reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing.
- Proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs, writing, or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs
- PV Project Management experience from ideally a service provider / CRO
- Health Care Professional or Life Science Graduate
- Be comfortable with communicating at senior levels within pharmaceutical organizations
- Have good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving.
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.