Site Budget Specialist I
我们是关心员工，客户，合作伙伴以及我们所做的工作质量的公司。一个动态的全球性公司成立于1995年，我们汇集了2700多名有志力，奉献和热情的人。我们在医学科学前线上工作，改变生活，并为需要者带来新药物。加入我们的拉特米团队作为创业团队的一部分，成为临床研究项目的主要支持者。你将在充满活力的多功能环境中工作，从各种与临床研究相关的学科获得独特技能。在哥伦比亚家庭职位。只会考虑英文简历。你将：· 审核和谈判现场预算 ·促进 PSI Legal,项目团队和研究地点之间的临床试验协议 (CTA) 和调查员补贴的审查和谈判 ·与 PSI Legal 合作定制并准备合同约束性网站特定文件 · 在临床试点管理系统 (CTMS) 中跟踪 CTA 和调查员补助谈判状态 ·编写可执行版本的合同，包括补助，协调签署过程 ·在试验主档中提交执行的合同并维护本地文档 ·与项目团队，翻译部门以及法律部门有关现场承包和补助谈论事务联系 · 支持研究初创团队的活动，如有需要 · 大学学位或同等教育，培训和经验结合 · 英语，语言和书面流利 · 与学习初创业务工作前经验是必需的 · 有资金和谈判经验；与临床试验网站相关法律文件的知识和经验将被视为一个附加之处 ·能够使用 MS Word,Excel 和 PowerPoint 的工作的 PC 技能 · 在动态的团队环境中规划和工作的能力 ·沟通和协作技巧 我们的使命是成为世界上最好的 CRO,根据我们的员工，客户，网站和供应商的测量。我们的招聘过程很简单，我们会随时陪伴你。
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We are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Join our LatAm team to be the key support to clinical research projects as part of the start-up team. You will work in a dynamic multi-functional environment, gaining unique skills from various disciplines relevant to clinical research.
Home-based position in Colombia.
Only CVs in English will be considered.
You will:
· Review and negotiate site budgets
· Facilitate the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site
· Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal
· Track CTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS)
· Prepare the executable version of the contract, including grants, and coordinates the signature process
· File executed contracts in the Trial Master File and maintains local documentation
· Liase with the project team, translation, and legal departments on site contracting and grant negotiation matters
· Support the activities of Study Startup team if needed
- College/University degree or an equivalent combination of education, training & experience
- Fluency in Spanish and English, oral and written
- Previous experience working with study startup operations is required
- Experience with finance and negotiation is desirable
- Knowledge and experience with legal documents related to clinical trial sites would be considered a plus
- PC skills to be able to work with MS Word, Excel and PowerPoint
- Ability to plan and work in a dynamic team environment
- Communication and collaboration skills
Our mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way.