Clinical Trial Operations Specialist

hace 1 mes

Xico, México Iqvia A tiempo completo

Job Overview

We are seeking a highly organized and detail-oriented Clinical Trial Operations Specialist to join our team at Iqvia. This is an exciting opportunity for someone with a passion for clinical research and excellent communication skills.

About the Role

In this role, you will be responsible for performing site activation activities in assigned studies, ensuring compliance with applicable regulations, standard operating procedures (SOPs), project requirements, and contractual guidelines. You will work closely with the Site Activation Manager, Project Management team, and other departments to ensure seamless execution of trial-related tasks.

Main Responsibilities:

  • Perform site activation activities in assigned studies, reviewing documents for completeness, consistency, and accuracy under guidance from 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 on the progress, 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 of experience in a healthcare environment or equivalent combination of education, training, and experience.
  • Productive individual contributor who works under general supervision.
  • Problems faced are generally routine but may require interpreting procedures or policies to resolve.
  • 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.

What We Offer:

This is an exciting opportunity to join a dynamic team and contribute to the success of our clients. As a Clinical Trial Operations Specialist at Iqvia, you can expect a competitive salary, benefits package, and opportunities for professional growth and development.

Salary Range:$60,000 - $80,000 per annum

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