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Clinical Trial Coordinator

hace 2 meses

Xico, México Iqvia A tiempo completo
Job Overview

As a key member of our team, you will perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements, and contractual/budgetary guidelines. This role may also involve maintenance activities.

Key Responsibilities
  • Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs, and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary.
  • Review documents for completeness, consistency, and accuracy, under guidance of senior staff.
  • Prepare site regulatory documents, reviewing for completeness and accuracy.
  • Inform team members of completion of regulatory and contractual documents for individual sites.
  • Distribute completed documents to sites and internal project team members.
  • Support the updating and maintenance of internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project-specific information.
  • Review, track, and follow up the progress, the approval, and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents.
Requirements
  • Bachelor's Degree in Life sciences or a related field.
  • 1 year's experience in a healthcare environment or equivalent combination of education, training, and experience.
  • Productive individual contributor who works under general supervision.
  • Good interpersonal communication and organizational skills.
  • Good attention to detail.
  • General awareness of the clinical trial environment and drug development process.
  • Ability to work on multiple projects.
  • Ability to establish and maintain effective working relationships with co-workers, managers, and sponsors.