Site Contract Specialist I

PSI CRO; São Paulo; Teletrabalho; BRL 90.000 - 130.000; Tempo integral

Resumo da oferta

A leading Contract Research Organization is seeking a candidate for their LatAm team in a home-based position in Brazil. The role involves supporting clinical research projects through tasks such as negotiating site budgets and contracts while providing opportunities for career advancement in a dynamic environment.

Serviços

Career advancement opportunities

Dynamic work environment

Training in various disciplines

Qualificações

• Previous experience in study startup operations required.
• Fluency in Portuguese and English required.
• Experience with finance and negotiation is desirable.

Responsabilidades

• Review and negotiate site budgets.
• Facilitate the negotiation of clinical trial agreements.
• Track negotiation status in the Clinical Trial Management System.

Conhecimentos

Communication

Collaboration

PC skills

Formação académica

College/University degree

Ferramentas

MS Word

Excel

PowerPoint

Descrição da oferta de emprego

Company Description

PSI is a leading Contract Research Organization with more than 27 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 tobe the key support to clinical research projects aspart of the start-up team. You willworkin 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 sitebudgets
• Facilitate the review and negotiation of clinical trial agreements (CTAs) and investigator grants between PSI Legal, the project team, and the study site
• Customizeand prepare contractually binding site-specific documents in cooperation with PSI Legal
• TrackCTA and investigator grant negotiation status in the Clinical Trial Management System (CTMS)
• Preparethe executable version of the contract, including grants, and coordinates the signature process
• Fileexecuted contracts in the Trial Master File and maintains local documentation
• Liasewith 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.