现场合同负责人 / 高级现场合同负责人
Global Site Contract Lead / Senior Site Contract Lead
当我们的价值观一致时，我们能够实现无限可能。
在Parexel，我们都有相同的目标——改善全球健康。从临床试验到监管、咨询和市场准入，我们提供的每项临床开发解决方案都基于一种特别的东西——对所做工作的深刻信念。
无论我们在Parexel做什么，每个人都在为最终能惠及患者的疗法开发做出贡献。我们认真对待工作，以同理心去做，并致力于带来改变。
职位简介
Parexel正在寻找一位经验丰富的全球站点合同负责人（SCL）/高级站点合同负责人（SSCL），以推动临床试验站点合同的卓越表现。这些职位需要有在面向发起方的背景下，领导多个国家和地区站点合同的经验。
您将负责整个合同生命周期——从策略和谈判到执行和绩效监控，同时优化流程、控制成本并管理风险。作为关键协调者，您将确保内部团队、发起方、站点和外部合作伙伴保持一致并专注于成功完成临床试验。
该职位远程办公，您必须居住在以下国家并拥有在该国工作的权利：
克罗地亚
捷克共和国
格鲁吉亚
匈牙利
立陶宛
波兰
罗马尼亚
塞尔维亚
乌克兰
您将负责
- 领导临床试验的端到端站点合同，确保及时有效地执行合同
- 监控并报告关键指标，包括周期时间、合同质量和合规性在整个合同生命周期中的表现
- 制定并实施合同策略文档、模板和最佳实践，以提高效率和一致性
- 与全球团队合作制定研究者资助预算和费用参数
- 管理特定项目的合同团队，提供领导力、培训和指导
- 识别并缓解与时间表、预算、策略有效性及质量相关的风险
- 与所有利益相关者保持透明沟通——发起方、内部团队、供应商、CRO和站点
- 建立并加强与内部和外部合作伙伴的关系，以加快合同执行
- 支持跨职能团队，包括临床运营、可行性、业务发展和研究者付款
- 向客户和高级管理层提供定期绩效更新和见解
- 确保准确
查看英文原文
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
About the Role
Parexel is seeking an experienced Global Site Contract Lead (SCL)/Senior Site Contract Lead (SSCL) to drive excellence in clinical trial site contracting. These levels require people with experience leading site contracting across multiple countries and regions in a sponsor-facing capacity
You'll oversee the complete contracting lifecycle—from strategy and negotiation through execution and performance monitoring—while streamlining processes, controlling costs, and managing risks. As a key orchestrator, you'll ensure internal teams, sponsors, sites, and external partners stay aligned and focused on delivering successful clinical trials.
The role is based remotely in the following countries which you must be living and have the right to work in:
Croatia
Czech Republic
Georgia
Hungary
Lithuania
Poland
Romania
Serbia
Ukraine
What You'll Do
- Lead end-to-end site contracting for clinical trials, ensuring timely and effective contract execution
- Monitor and report on critical metrics including cycle times, contract quality, and compliance throughout the contract lifecycle
- Develop and implement contracting strategy documents, templates, and best practices that drive efficiency and consistency
- Collaborate with global teams on investigator grant budgets and fee parameters
- Manage project-specific contracting teams, providing leadership, training, and mentorship
- Identify and mitigate risks related to timelines, budgets, strategy effectiveness, and quality
- Maintain transparent communication with all stakeholders—sponsors, internal teams, vendors, CROs, and sites
- Build and strengthen relationships across internal and external partners to expedite contract execution
- Support cross-functional teams including Clinical Operations, Feasibility, Business Development, and Investigator Payments
- Provide regular performance updates and insights to clients and senior management
- Ensure accurate budget tracking and resource forecasting for the contracting team
What We're Looking For
- Very strong global site contracting experience within a CRO or other clinical research setting.
- Experience leading site contracting across multiple countries and regions
- Bachelor's degree in law, business, economics, or related field (or equivalent industry experience)
- Strong negotiation and contract management skills with ability to interpret complex legal language
- Excellent leadership, diplomacy, and interpersonal skills with proven ability to influence across teams
- Outstanding organizational and project management abilities—comfortable juggling multiple concurrent projects
- Advanced proficiency in Excel, Word, and PowerPoint
- Strong analytical skills and attention to detail
- Experience with contract management systems and eTMF platforms
- Ability to thrive in virtual, multicultural, and cross-timezone environments
- Demonstrated thought leadership, problem-solving ability, and grace under pressure
Why Join Us?
You'll take ownership of a critical function that directly impacts trial success, working with talented cross-functional teams and gaining exposure to diverse therapeutic areas and global operations.
Originally posted on Himalayas