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Clinical Trial Coordinator

TN France

France

Sur place

EUR 30 000 - 60 000

Plein temps

Il y a 19 jours

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Résumé du poste

An innovative firm is seeking a Clinical Trial Coordinator to support project teams in managing clinical trials. This role involves reviewing regulatory documents, liaising with investigative sites, and coordinating team activities. Ideal candidates will have strong administrative skills, proficiency in Microsoft Office, and a keen attention to detail. Join a dedicated team that plays a crucial role in accelerating the delivery of life-saving therapies, contributing to a healthier, cleaner, and safer world.

Qualifications

  • Previous administrative experience is essential.
  • Knowledge of clinical research is a plus.

Responsabilités

  • Review regulatory documents and perform investigator file reviews.
  • Liaise with monitors and resolve regulatory issues.

Connaissances

Administrative Experience
Clinical Research Knowledge
Microsoft Office Proficiency
English Language Skills
Attention to Detail
Social Skills

Outils

Project Tracking Tools

Description du poste

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About Thermo Fisher Scientific

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Our Role

We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD clinical research services - thousands of employees worldwide, connected by tenacity and passion for our purpose: to accelerate the delivery of life-saving therapies to patients.

Position Overview

As a Clinical Trial Coordinator, you will support the Project Team by providing administrative and technical support for site activities and coordinating various clinical trials across therapeutic areas.

Key Responsibilities
  1. Review regulatory documents for proper content.
  2. Perform investigator file reviews and log outstanding issues in project tracking tools.
  3. Liaise with monitors and investigative sites to resolve regulatory issues.
  4. Disseminate study-related information, including project updates, to clients, study teams, and departments.
  5. Assist in identifying potential investigators and developing/distributing initial protocol packets.
  6. Create meeting agendas and minutes.
  7. Coordinate team conference calls and distribute meeting minutes.
Qualifications
  • Previous administrative experience.
  • Knowledge or experience in clinical research is advantageous.
  • Proficiency in Microsoft Office suite.
  • Excellent English language and grammar skills.
  • Strong social skills, attention to detail, and ability to handle multiple tasks efficiently.
Additional Information

Please submit your CV in English. You must be located in France for this opportunity.

Our Mission and Values

Our mission is to enable our customers to make the world healthier, cleaner, and safer. We are a team of over 100,000 colleagues sharing values of Integrity, Intensity, Innovation, and Involvement, working together to accelerate research, solve scientific challenges, and support patients in need.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and values diversity in backgrounds and perspectives.

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