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We are seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team at Thermo Fisher Scientific. In this role, you will be responsible for coordinating and overseeing trial activities, ensuring timely completion of tasks, and maintaining high-quality standards.
Key Responsibilities- Coordinate and oversee trial activities, including department, internal, country, and investigator file reviews.
- Ensure allocated tasks are performed on time, within budget, and to a high-quality standard.
- Proactively communicate any risks to project leads and support the maintenance of study-specific documentation and systems.
- Provide system support, including GoBalto and eTMF, and support RBM activities.
- Perform administrative tasks, including timely processing of documents, performing eTMF reviews, and providing documents and reports to internal team members.
- Support scheduling of client and/or internal meetings, reviews and tracks local regulatory documents, and transmits documents to client and centralized IRB/IEC.
- Analyze and reconcile study metrics and findings reports, and assist with clarification and resolution of findings related to site documentation.
- Maintain vendor trackers, assist with coordination, compilation, and distribution of Investigator Site File (ISF) and Pharmacy binder materials, and assist with study-specific translation materials and translation QC.
- High/Secondary school diploma or equivalent and relevant formal academic/vocational qualification. Bachelor's degree preferred.
- Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).
At Thermo Fisher Scientific, we offer a dynamic and supportive work environment, opportunities for professional growth and development, and a competitive compensation package.