瑞士总部 - 赞助专用站点预算与合同专员
Sponsor Dedicated Site Budget & Contract Specialist based in Switzerland
加入我们的团队，塑造临床研究的未来！
在Fortrea，我们致力于简化临床试验并确保符合全球法规。作为站点预算与合同专员（地点：瑞士；远程办公），您将在协商和管理站点协议、保密协议和其他关键合同方面发挥关键作用，以支持我们的临床研究工作。您的工作将有助于推动突破性研究的成功，同时确保合规性和效率。
在此职位中，您将加入我们的FSP团队，并直接与我们著名的主要赞助商合作，推进创新、改变生命的药物开发。
主要职责：
在此职位中，您将：
- 准备、协商并管理临床试验的站点协议、保密协议和赔偿函。
- 确保符合SOP、监管指南和合同义务。
- 跟踪、更新并维护相关系统中的合同状态，确保透明度和及时执行。
- 在需要时将合同问题上报给管理层。
- 支持合同的内部审核、修订和审批流程，然后再转发给外部方。
- 与临床研究团队、法务和项目管理团队协作，确保合同顺利执行。
- 维护电子和纸质合同文件，确保准确性和可访问性。
- 协助部门流程和程序的持续改进。
- 向管理层和研究团队提供定期状态更新。
所需资格：
要在此职位上取得成功，您应具备：
- 本科学位（LLB、JD、BA或BS）优先；大学法律学位非常受欢迎。
- Fortrea可能会考虑用相关经验替代教育要求。
- 2-4年合同谈判、临床研究或相关领域的经验。
- 对ICH GCP指南和临床研究流程有深入了解。
- 优秀的谈判、沟通和组织能力。
- 能够独立工作，并在快节奏环境中管理多项优先任务。
- 熟练使用Microsoft Office和合同跟踪系统。
- 德语和英语流利
我们提供的福利：
- 竞争力的薪资和绩效激励。
- 灵活的工作安排
- 在协作和创新环境中的职业发展机会。
- 有机会参与
查看英文原文
Join Our Team and Shape the Future of Clinical Research!
At Fortrea, we are dedicated to streamlining clinical trials and ensuring compliance with global regulations. As a Site Budget & Contract Specialist (location: Switzerland; Home-Based), you will play a critical role in negotiating and managing site agreements, confidentiality agreements, and other key contracts that support our clinical research efforts. Your work will help drive the success of groundbreaking studies while ensuring compliance and efficiency.
In this role, you will be part of our FSP team and work directly with one of our renowned key sponsor to advance the development of innovative, life-changing medications.
Key Responsibilities:
In this role, you will:
- Prepare, negotiate, and manage site agreements, confidentiality agreements, and letters of indemnification for clinical trials.
- Ensure compliance with SOPs, regulatory guidelines, and contractual obligations.
- Track, update, and maintain contract status in relevant systems, ensuring transparency and timely execution.
- Identify and escalate contractual issues to management as needed.
- Support the internal review, revision, and approval process of contracts before forwarding them to external parties.
- Collaborate with clinical study teams, legal, and project management to ensure seamless contract execution.
- Maintain electronic and paper contract files, ensuring accuracy and accessibility.
- Assist in the continuous improvement of departmental processes and procedures.
- Provide regular status updates to management and study teams.
Required Qualifications:
To succeed in this role, you should have:
- Bachelor’s degree (LLB, JD, BA, or BS) preferred; a university-level law degree is highly desirable.
- Fortrea may consider equivalent relevant experience in lieu of educational requirements.
- 2-4 years of experience in contract negotiation, clinical research, or a related field.
- Strong understanding of ICH GCP guidelines and clinical research processes.
- Excellent negotiation, communication, and organizational skills.
- Ability to work independently and manage multiple priorities in a fast-paced environment.
- Proficiency in Microsoft Office and contract tracking systems.
- Fluent in German and in English
What We Offer:
- Competitive salary and performance-based incentives.
- Flexible work arrangements
- Professional growth opportunities in a collaborative and innovative environment.
- The opportunity to work on cutting-edge clinical research projects.
Ready to Make an Impact?
Take the next step in your career and join us in driving innovation in clinical research.
Apply today! Applications are reviewed on a rolling basis—don’t miss this opportunity!
Learn more about our EEO & Accommodations request here.
Originally posted on Himalayas