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Clinical Trial Coordinator - Madrid

  • Job
    Full-time
    Entry Level
  • Research & Development
    Healthcare
  • Madrid

AI generated summary

  • You need a university degree or equivalent, strong analytical skills, experience managing multiple projects, excellent communication and organization abilities, and fluency in Spanish and English.
  • You will review investigator files and regulatory documents, resolve issues with sites, disseminate study information, assist in identifying investigators, and coordinate meetings and agendas.

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

Responsibilities

  • Performs 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

FAQs

What is the job title for this position?

The job title is Clinical Trial Coordinator.

Where is this position located?

This position is located in Madrid.

What type of work environment can I expect?

The work environment is primarily office-based.

What qualifications are required for this role?

A university degree or equivalent in education, training, and experience is required.

Is fluency in any specific languages necessary for this position?

Yes, fluency in both Spanish and English is essential.

What are the main responsibilities of a Clinical Trial Coordinator?

Key responsibilities include performing investigator file reviews, reviewing regulatory documents, liaising with monitors and investigative sites, disseminating study-related information, assisting with identifying potential investigators, and coordinating meeting agendas and conference calls.

How does Thermo Fisher Scientific support work-life balance?

Thermo Fisher Scientific promotes a flexible working culture that values work-life balance.

Does the company offer benefits?

Yes, the company has an extensive benefits package focused on the health and well-being of employees.

How can I submit my application for this role?

You can submit your CV in English.

Are there opportunities for professional development within the company?

Yes, Thermo Fisher Scientific provides resources to achieve individual career goals and fosters a collaborative environment.

The World Leader In Serving Science

Science & Healthcare
Industry
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Employees

Mission & Purpose

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.