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Clinical Trial Coordinator
hace 2 meses
Fortrea is seeking a highly motivated and organized Sr Clinical Trial Coordinator to join our team. As a key member of our clinical operations team, you will be responsible for coordinating and managing clinical trials from start to finish.
Responsibilities:- Coordinate and manage site contacts, including creating contact reports and monitoring site performance.
- Assist CRAs with preparation for site visits, including running reports and QC of files.
- Perform Case Report Form review, query generation and resolution against established data review guidelines.
- Coordinate study visits and shipment of drug, ancillary supplies and laboratory kits/samples.
- Manage sites to ensure subjects are complying with protocol requirements, study visits, and timelines.
- Liaise with the project team and others to distribute and track clinical trial supplies.
- Proactively work with sites and project teams to ensure maintenance activities are completed.
- Demonstrate an understanding of CTMS and enter weekly details as required.
- Assist in submissions and notifications to Ethics Committees and Regulatory Authorities.
- Facilitate translation and back translation of necessary documents as required.
- Previous experience with Logistics / Imports / Supplies within CRO environment.
- Completed job training or Bachelor's Degree.
- Advanced English.
- Good IT skills, including MS Office and MS Excel.
- Hands-on profile.
Fortrea is a leading global contract research organization with a passion for scientific rigor and decades of clinical development experience. We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
