Clinical Trial Coordinator

hace 1 día

Xico, México Thermo Fisher Scientific A tiempo completo
{"title": "Clinical Trial Coordinator", "content": "Job Summary

We are seeking a highly organized and detail-oriented Clinical Trial Coordinator to join our team. As a Clinical Trial Coordinator, you will provide administrative and technical support to the Project Team, ensuring the smooth execution of clinical studies.

Key Responsibilities:

  • Review regulatory documents for proper content
  • Perform study investigator file reviews and logging of outstanding issues in project-related tracking tools
  • Liaise with monitor and investigative sites to resolve outstanding regulatory issues identified
  • Disseminate study-related information, including project tracking updates to Clients, clinical study teams, and other PPD/TFS departments
  • Assist Project Leads and Functional Leads with execution/facilitation of crucial tasks and deliverables to expedite resolution and/or updates
  • Provide tracking of training matrices, SOP lists, and completion adherence and requirements
  • Attend high-profile conference calls with Clients and provide sufficient response to inquiries

Requirements:

  • 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)
  • Knowledge, Skills, and Abilities:
    • Ability to work in a team or independently as required
    • Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
    • 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 non-clinical/clinical aspects of project implementation, execution, and closeout
    • Good English language and grammar skills and proficient local language skills as needed
    • Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
    • Ability to successfully complete PPD clinical training program
    • Self-motivated, positive attitude, and good interpersonal skills

Working Environment:

PPD part of TFS values the health and wellbeing of our employees. We support and encourage individuals to create a healthy and balanced environment where they can thrive.

PPD/TFS 4i Values:

Integrity Innovation Intensity Involvement

"}

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