Clinical Trials Coordinator Professional

hace 12 horas


Buenos Aires, Buenos Aires C.F., Argentina CDS Fortrea Inc. A tiempo completo

Seeking a highly motivated and detail-oriented Clinical Trials Coordinator to join our team at CDS Fortrea Inc. in New Roles.

About the Role:

We are looking for a skilled professional with experience in logistics, imports, and supplies within a contract research organization (CRO) environment.

The successful candidate will be responsible for coordinating clinical trials, including managing sites, ensuring subject compliance with protocol requirements, and facilitating communication between project teams and investigative sites.

Key Responsibilities:
  • Serve as primary contact for project teams and investigative sites, conducting site contacts and documenting interactions as required by study guidelines.
  • Monitor site performance and implement action plans for underperforming sites in collaboration with CRAs.
  • Assist CRAs with preparation for site visits, including running reports, quality checking files, and resolving outstanding issues from previous visits.
  • Perform Case Report Form reviews, query generation, and resolution against established data review guidelines on Covance or client data management systems, as assigned by management.
  • Coordinate study visits, shipments of drug, ancillary supplies, and laboratory kits/samples.
  • Manage sites to ensure subjects comply with protocol requirements, study visits, and timelines.
  • Liaise with project teams and others to distribute and track clinical trial supplies, such as Case Report Forms, study medication, lab kits, to ensure sites have sufficient materials for ongoing recruitment.
  • Work proactively with sites and project teams to complete maintenance activities, including Amendments, revised documents, as applicable in the region.
  • Demonstrate an understanding of CTMS, its purpose, use, and navigation within different sections, entering weekly details as required.
  • Assist with submissions and notifications to Ethics Committees and Regulatory Authorities, as applicable in the region.
  • Facilitate translation and back-translation of necessary documents for local country requirements and regional needs.
Requirements:
  • Prior experience working in logistics, imports, or supplies within a CRO environment.
  • Completed job training in office management, administration, finance, or healthcare, or a Bachelor's Degree.
  • Advanced English proficiency.
  • Strong IT skills, including MS Office and Excel.
  • A hands-on approach to work.
Benefits:

CDS Fortrea Inc. offers a competitive salary, estimated at around $60,000 - $80,000 per year, depending on location and experience. Additionally, we provide opportunities for personal growth, a collaborative work environment, and the chance to make a meaningful global impact in the field of clinical trials.



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