Ofertas de empleo en PSI CRO AG

• Nivel de experiencia---
• Tipo de contratoA tiempo completo
• PublicadaNueva

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

Join our international team and be the key support to clinical research projects, as part of the start-up team, working in a dynamic multi-functional environment, gaining unique skills from various disciplines relevant to clinical research.

This is an office-based position in Madrid, Spain.

You will:

• Coordinate review and negotiation of clinical trial agreements and investigator grants between PSI staff and Spanish study sites.
• Perform administrative activities (documents collection/distribution, filing clinical trial agreements in the database and maintenance of local documentation).
• Customize and prepare contractually binding site-specific documents in cooperation with PSI Legal.
• Prepare the executable version of the contract and coordinate the signature process.
• Update and maintain relevant tracking and filing systems.
• Liaise with project teams and other PSI departments on site contracting and grant negotiation matters.
  
  
  

• College/University degree or an equivalent combination of education, training and experience
• Prior industry experience in clinical research
• Prior experience with legal documents related to clinical trial sites is a plus
• Full working proficiency in Spanish and English
• Communication and organizational skills
• Attention to detail and ability to plan, multitask and work in a dynamic team environment
  
  
  

• Excellent working conditions
• Extensive training and friendly team
• Competitive salary and benefits package