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Site Contract Specialist I

PSI CRO

Brazilfull-timePosted 17 day(s) ago$0-$0 / yr

$0-$0 / yr

Salary

brazil

Region

ASAP

Start Date

About PSI CRO

PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

About this Role.

Company Description PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description 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 Brazil. 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 Qualifications * College/University degree or an equivalent combination of education, training & experience * 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 * Fluency in Portuguese and English, oral and written Additional Information Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with the company.

Skills Required

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