高级合同谈判官（FSP）- 德语使用者，居家办公在德国
Senior Contract Negotiator (FSP) - German speaker, Home based in Germany
核心职责
- 开发并协调研究者资助和估算的开发，制定合同策略和提案文本以支持提案开发流程。
- 根据职位要求，开发合同条款、付款条款和预算模板
- 根据工作范围和项目计划，在约定的项目策略内，使用并维护选定赞助方、研究或多项协议项目的合同系统、工具、流程和培训材料。
- 确保协作，包括与赞助方、利益相关者和RSU区域及国家的沟通，以符合赞助方要求和/或RSU管理计划，成功交付约定的项目范围。
- 为研究团队提供专业法律、运营和财务合同支持，适用于站点协议，以促进高效的业务开发和临床试验的启动与维护，同时确保符合监管要求。
- 确保整体合同效率，遵守项目时间表和财务目标，适用于站点协议
- 按要求报告合同绩效指标和超出范围的合同活动。
- 与质量管理团队合作，确保适当的合同管理和质量标准。根据需要指导和辅导同事，包括按需提供培训材料。
任职资格
- 相关领域的学士学位 或 5年相关的赞助方或临床研究组织临床站点合同经验
- 良好的谈判和沟通能力，能够提出挑战
- 强大的法律、财务和/或技术写作能力
- 对受监管的临床试验环境有深入了解，并了解药物开发流程
- 对临床试验合同管理有良好的理解
- 英语和德语流利
IQVIA是生命科学和医疗行业临床研究服务、商业洞察和医疗健康智能领域的全球领先提供商。我们创造智能连接，加速创新医疗方案的研发和商业化，帮助改善全球患者的预后和人群健康。了解更多，请访问
IQVIA致力于在招聘过程中保持诚信，对候选人欺诈采取零容忍政策。您提交的所有信息和资质均将被严格审核。
查看英文原文
Essential Functions
- Develop Coordinate the development of investigator grants and estimates, contracting strategies and proposal text to support the proposal development process.
- Develop contract language, payment language and budget templates as required as applicable to the position
- Utilize and maintain contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.
- Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries as applicable to the position, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
- Provide specialist legal, operational and financial contracting support to the Study Teams, as applicable to site agreements to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
- Ensure overall contracting efficiency and adherence to project timelines and financial goals as applicable to site agreements
- Report contracting performance metrics and out of scope contracting activities as required.
- Work with Quality Management to ensure appropriate contract management and quality standards. Mentor and coach colleagues as required including the delivery of training materials as required.
Qualifications
- Bachelor's Degree Related field OR 5-year relevant sponsor or clinical research organization clinical site contracting experience
- Good negotiating and communication skills with ability to challenge.
- Strong legal, financial and/or technical writing skills.
- Strong understanding of regulated clinical trial environment and knowledge of drug development process.
- Good understanding of clinical trial contract management.
- Fluent in English and German language
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Originally posted on Himalayas