Clinical Trial Coordinator - client-dedicated

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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:

1

Posted:

25.04.2025

Expiry Date:

09.06.2025

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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 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.

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 in locations worldwide connected by tenacity and passion for our purpose: to. You will be joining a truly as we strive to bend the time and cost curve of delivering life-saving therapies to patients.

As a Clinical Trial Coordinator, you will play an integral role supporting the Project Team. You will be able to provide administrative and technical support for site activities and coordinate a variety of exciting trials in various therapeutic areas!

Key responsibilities of the Clinical Trial Coordinator are:

• Review regulatory documents for proper content
• Perform PPD investigator file reviews and log outstanding issues in project-related tracking tools
• Liaise with monitor and investigative sites to resolve regulatory issues
• Disseminate study-related information, including project tracking updates to clients, study teams, and other departments
• Assist with identifying potential investigators and developing/distributing initial protocol packets
• Create meeting agendas and minutes
• Coordinate team conference calls and distribute meeting minutes

Skills and experience required:

• Some previous administration experience
• Clinical research knowledge or experience is a plus
• Proficiency in Microsoft Office suite
• Excellent English language and grammar skills
• Strong social skills and high attention to detail, with the ability to handle multiple tasks efficiently

Please submit your CV in English.

Location requirement: You must be located 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 share core values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve scientific challenges, drive innovation, and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences and perspectives are valued.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, disability, or any other protected class.