Study Site Specialist

2 weeks ago


Pretoria, Gauteng, South Africa IQVIA Argentina Full time

Project Overview

IQVIA Argentina is currently seeking a Study Site Specialist to join our team. As a key member of our team, you will be responsible for executing site activation activities in accordance with regulations, SOPs, and project requirements at the regional or country level. This includes preparing and managing site documentation, reviewing and negotiating site documents and contracts, and maintaining, reviewing, and reporting on site performance metrics.

Responsibilities

  • Serve as a Single Point of Contact (SPOC) to perform feasibility, site activation, and some maintenance activities in assigned studies for investigative sites.
  • Prepare site documents, reviewing for completeness and accuracy.
  • Inform team members of the completion of regulatory, contractual, and other documents for individual sites.
  • Distribute completed documents to sites and internal project team members.
  • Update and maintain 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 required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents.

Qualifications

  • Bachelor's Degree in Life Sciences or a related field required.
  • 1 - 3 years' clinical research or other relevant experience; or equivalent combination of education, training, and experience required.
  • 3 years' experience in a healthcare environment or equivalent combination of education, training, and experience required.
  • Languages: English and Italian.


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