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Clinical Trial Coordinator FSP LATAM

hace 2 meses


Bogotá, Bogotá D.E., Colombia Thermo Fisher Scientific A tiempo completo
Job Summary

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team at Thermo Fisher Scientific. As a Clinical Trial Coordinator, you will play a critical role in the success of our clinical trials by providing administrative and technical support to our project teams.

Key Responsibilities
  • Administrative Support: Provide administrative support to project teams, including coordinating tasks, managing files, and ensuring compliance with organizational SOPs and department guidance documents.
  • Audit Readiness: Ensure files are reviewed according to the schedule detailed in the organization's SOP and department guidance document to support audit readiness.
  • Site Activation: Provide administrative support for site activation activities, including coordinating with sites, managing documents, and ensuring compliance with regulatory requirements.
  • Critical Path Development: Aid in the development of the critical path for site activation within assigned projects in support of rapid site activations.
  • Represent CRG Personnel: Represent CRG personnel and provide local input into the site tiering process.
  • Communication and Collaboration: Communicate with project teams, sites, and other stakeholders to ensure effective collaboration and coordination.
  • Documentation and Record-Keeping: Maintain accurate and up-to-date records of project activities, including site contact and follow-up information.
  • Training and Development: Provide training to new staff as needed and contribute to the development of global strategic feasibility processes and best practices.
Requirements
  • Education: High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification. Bachelor's degree preferred.
  • Experience: Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year). In some cases, an equivalency, consisting of a combination of appropriate education, training, and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
  • Skills and Abilities: Ability to work in a team or independently as required; good organizational skills and strong attention to detail; demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency; strong customer focus; flexibility to reprioritize workload to meet changing project timelines; demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all nonclinical/clinical aspects of project implementation, execution, and closeout.
Working at Thermo Fisher Scientific

At Thermo Fisher Scientific, we are committed to helping our customers make the world healthier, cleaner, and safer. As a Clinical Trial Coordinator, you will be part of a dynamic team that is dedicated to delivering high-quality clinical trials and making a meaningful impact in the lives of patients and communities around the world.