Clinical Trial Coordinator - client-dedicated

Thermo Fisher Scientific; Ivry-sur-Seine; Sur place; EUR 35 000 - 50 000; Plein temps

Résumé du poste

Join a leading company as a Clinical Trial Coordinator in Ivry-sur-Seine. You will play a key role in facilitating clinical trials, ensuring regulatory compliance, and supporting project teams. Your administrative skills and attention to detail will be essential in improving health outcomes globally.

Qualifications

• Some administrative experience required.
• Knowledge or experience in clinical research is advantageous.
• Excellent English language skills needed.

Responsabilités

• Review regulatory documents for accuracy and completeness.
• Coordinate with monitors and investigative sites.
• Prepare meeting agendas and minutes.

Connaissances

Attention to Detail

Multitasking

Social Skills

Outils

Microsoft Office

Description du poste

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Clinical Trial Coordinator - client-dedicated, Ivry-sur-Seine

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Client:

Thermo Fisher Scientific

Location:

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

111b0115b893

Job Views:

5

Posted:

21.06.2025

Expiry Date:

05.08.2025

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Job Description:

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 advancing science through research, development, and delivery of life-changing therapies. Our clinical trials are conducted in over 100 countries, and we are continuously developing new frameworks for clinical research through our PPD portfolio, spanning laboratory, digital, and decentralized services. Your dedication to quality and accuracy will contribute to improving health outcomes for communities worldwide.

We are the vital link between a new medicine idea and the people who need it. As part of PPD clinical research services, we are thousands of employees worldwide united by our passion and purpose: to accelerate the delivery of life-saving therapies to patients.

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

Key responsibilities:

• Review regulatory documents for accuracy and completeness
• Conduct investigator file reviews and log issues in tracking tools
• Coordinate with monitors and investigative sites to resolve regulatory issues
• Distribute study information and updates to clients and teams
• Assist in identifying investigators and preparing protocol packets
• Prepare meeting agendas and minutes
• Coordinate conference calls and share minutes

Requirements:

• Some administrative experience
• Knowledge or experience in clinical research is advantageous
• Proficiency in Microsoft Office suite
• Excellent English language skills
• Strong social skills and attention to detail, with the ability to multitask effectively

Please submit your CV in English.

Location requirement: You must be based in France for this opportunity.

Our Mission is to enable our customers to make the world healthier, cleaner, and safer. As a team of over 100,000 colleagues, we value integrity, intensity, innovation, and involvement—working together to accelerate research, solve scientific challenges, drive innovation, and support patients. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse backgrounds and perspectives are valued.

Thermo Fisher Scientific is an equal opportunity employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or other protected categories.