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Site Contract Specialist - Remote

Posted 3 days ago
All others
Full Time
Turkey

Overview

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.

In Short

  • Coordinate review and negotiation of clinical trial agreements and investigator grants.
  • Perform administrative activities such as document collection and filing.
  • Customize and prepare site-specific documents in cooperation with PSI Legal.
  • Prepare executable versions of contracts and coordinate the signature process.
  • Update and maintain relevant tracking and filing systems.
  • Liaise with project teams on site contracting and grant negotiation matters.

Requirements

  • College/University degree or equivalent combination of education and experience.
  • Prior industry experience in clinical research.
  • Experience with legal documents related to clinical trial sites is a plus.
  • Full working proficiency in Turkish and English.
  • Strong communication and organizational skills.
  • Attention to detail and ability to multitask.
  • Ability to work in a dynamic team environment.

Benefits

  • Opportunity to grow in clinical research career.
  • Enhance communication skills.
  • Work in a dynamic multi-functional environment.
PSI CRO logo

PSI CRO

PSI CRO is a prominent Contract Research Organization (CRO) with over 25 years of experience in the pharmaceutical industry. Founded in Switzerland, PSI is a privately owned, full-service CRO that operates globally, supporting clinical trials across various countries and continents. The company is known for its selective approach to project engagement, emphasizing high-quality and timely services across a wide range of therapeutic areas. PSI values diversity and inclusivity within its workforce, fostering an environment where all colleagues feel welcomed and valued. The organization is dedicated to not only conducting clinical trials but also building a community that empowers team members to thrive and contribute to significant advancements in the pharmaceutical sector.

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