账户专员（临床试验）
Site Management Associate (Clinical Trials)
我们是一家注重员工、客户、合作伙伴以及工作质量的公司。一家成立于1995年的动态全球企业，我们汇聚了3000多名有动力、有奉献精神且充满热情的个人。我们在医学科学的最前沿工作，改变生命，并为需要的人带来新药。
此远程职位面向荷兰任何地区的候选人开放。
这是一个绝佳的机会，可以建立广泛的临床运营经验，直接与研究站点和国际项目团队合作，并在临床研究领域进一步发展。
职责范围包括：
· 在临床研究项目中作为研究站点的关键联系人。
· 支持站点有效开展日常临床研究工作，确保及时沟通和跟进。
· 协调解决站点特定问题，并促进站点、项目团队和其他相关方之间的协作。
· 为站点团队提供项目培训，并协助访问研究相关和供应商系统。
· 跟踪研究和站点活动，跟进未完成事项，并帮助保持项目进度。
· 在相关系统中维护准确的研究信息，并确保必要文件完整且最新。
· 协调内部团队和外部合作伙伴之间的信息和沟通。
· 通过起草议程、记录会议纪要和跟进已达成的行动项来支持项目会议。
- 至少6个月的临床研究经验
- 生命科学相关学位
- 全面的专业英语和荷兰语能力
- 良好的组织和规划能力
- 注重细节，能够多任务处理，并在快节奏环境中高效工作
- 良好的解决问题能力和灵活性
- 以团队合作为导向，具备优秀的客户服务和人际交往能力，对任务和项目有积极的态度
- 熟练使用标准的MS Office应用（Word、Excel和PowerPoint）
做出正确的选择，将你的职业生涯提升到全新高度。加入这家关注员工并投资于其职业发展和成功的公司。
查看英文原文
We are the company that cares; for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
This remote position is open to candidates based anywhere in the Netherlands.
This is an excellent opportunity to build broad clinical operations experience, working directly with investigative sites and international project teams, with opportunities to develop further within clinical research.
The scope of responsibilities will include:
· Serve as a key point of contact for investigative sites throughout clinical research projects.
· Support sites in the effective day-to-day delivery of clinical studies, ensuring timely communication and follow-up.
· Coordinate resolution of site-specific questions and facilitate collaboration between sites, project teams and other stakeholders.
· Support site teams with project training and access to study-related and vendor systems.
· Track study and site activities, follow up on outstanding actions and help keep projects on schedule.
· Maintain accurate study information in relevant systems and ensure essential documentation is complete and up to date.
· Coordinate information and communication across internal teams and external partners.
· Support project meetings by drafting agendas, taking minutes, following up on agreed actions.
- At least 6 months of experience within clinical research
- Life Sciences degree
- Full professional working proficiency in Dutch and English
- Good organizational and planning skills
- Detail-oriented, able to multi-task and work effectively in a fast-paced environment
- Good problem-solving abilities, flexibility
- Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects
- Proficiency in standard MS Office applications (Word, Excel and PowerPoint)
Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.