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 Argentina.
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
Requirements:
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.
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📌 Site Budget Specialist I (Buenos Aires)
🏢 Psicro
📍 Buenos Aires