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Clinical Trial Coordinator
Il y a 3 mois
Work Schedule
Other
Environmental Conditions
Office
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 improve health ) . You will be joining a truly collaborative and winning culture ) 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:
- Reviews of regulatory documents for proper content
- Performs PPD investigator file reviews and logging of outstanding issues in project related tracking tools
- 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
- Coordinates team conference calls and distribution of meeting minutes
To be considered for this exciting opportunity you will require the following skills and experience:
- Some previous administration experience.
- Clinical research knowledge or experience will be seen as an advantage.
- Working skills across all of the Microsoft packages
- Excellent English language and grammar skills
- Strong social skills and high attention for detail, with proven track record to handle multiple tasks efficiently and effectively
Please submit your CV in English.
You have to be located in France for this opportunity.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
