Clinical Research Associate
hace 4 semanas
Job Summary
As a Clinical Trial Coordinator at Thermo Fisher Scientific, you will play a critical role in supporting the success of our clinical trials. You will provide technical support to the project team, coordinating non-clinical responsibilities of project administration as applicable to the client contract.
Key Responsibilities
- Perform investigator file reviews and logging of outstanding issues in project related tracking tools
- Review regulatory documents for proper content
- Liaise with monitor and investigative sites to resolve outstanding regulatory issues identified
- Disseminate study related information, including project tracking updates to Clients, clinical study teams and other PPD departments
- Assist with the identification of potential investigators and development/distribution of initial protocol packets
- Create meeting agendas and minutes, as well as coordinate team conference calls and distribution of meeting minutes
Qualifications
- University degree, or equivalent in education, training and experience
- Ability to effectively analyze project specific data/systems to ensure accuracy and efficiency
- Experience of managing multiple projects with differing priorities at one given time
- Exceptional communication, collaboration, organizational and time management skills
- Fluency in Spanish and English is essential
What We Offer
- A competitive salary
- An extensive benefits package based around the health and well-being of our employees
- A flexible working culture, where PPD clinical research services truly value a work-life balance
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