Clinical Research Coordinator

hace 4 semanas


Barcelona, Barcelona, España Thermo Fisher Scientific A tiempo completo

About the Role:

As a Clinical Trial Coordinator at Thermo Fisher Scientific, you will play a crucial role in supporting the project team by coordinating non-clinical responsibilities of project administration. This includes performing investigator file reviews, logging outstanding issues, and reviewing regulatory documents for proper content.

Key Responsibilities:

  • Perform investigator file reviews and logging of outstanding issues in project related tracking tools
  • Reviews regulatory documents for proper content
  • Liaises with monitor and investigative sites to resolve outstanding regulatory issues identified
  • Disseminates study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
  • Assists with the identification of potential investigators and development/distribution of initial protocol packets
  • Creates meeting agendas and minutes, as well as coordinates team conference calls and distribution of meeting minutes

Requirements:

  • University degree, or equivalent in education, training and experience
  • Ability to effectively analyse project specific data/systems to ensure accuracy and efficiency
  • Experience of manage multiple projects with differing priorities at one given time
  • Exceptional communication, collaboration, organisational and time management skills
  • Fluency in Spanish and English is essential

What We Offer:

As a valued member of our team, you will be rewarded with a competitive salary and an extensive benefits package based around the health and well-being of our employees. We offer a flexible working culture, where PPD clinical research services truly value a work-life balance.

We are a global organisation but with a local feel. Our Mission is to enable our customers to make the world healthier, cleaner and safer.

How to Apply:

Please submit your CV in English.



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