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Clinical Trial Coordinator
Remote · Argentina
Job Summary
Coordinate and facilitate clinical trial activities across assigned trials, supervising documentation, training, and cross-functional collaboration. Act as a study lead when needed, manage (e)TMF-related tasks, provide system support (GoBalto & eTMF), support RBM activities, handle meeting scheduling and minutes, review regulatory documents, and assist with translation materials and QC. Demonstrates strong organizational skills, attention to detail, and the ability to work independently or in a team, with proficiency in MS Office and clinical trial database systems, while ensuring tasks are completed on time and within budget. May require occasional travel and work in an office/home-office environment. Thermo Fisher Scientific and its brands are equal opportunity employers. Please contact for accommodations during the application process.
Required Qualifications
- High/Secondary school diploma or equivalent and relevant formal academic/vocational qualification
- Bachelor's degree preferred
- 4+ years of related experience or equivalent
- Ability to work in a team or independently
- Strong organizational skills and attention to detail
- Knowledge of ICH GCP and regulatory requirements
- Proficiency in MS Office (Word, Excel, PowerPoint) and clinical trial databases
- Ability to manage multiple tasks and meet timelines
- Experience with eTMF and GoBalto systems
- Strong communication and training skills
- Fluent in English; local language skills as needed
- Ability to travel as required
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