IQVIA

Site Activation Specialist, Client Dedicated (Contract)

IQVIA(1 month ago)

HybridFull TimeJunior$61,214 - $81,704 (estimated)Clinical Operations
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About this role

This is a contract role supporting clinical trial site feasibility and activation activities at a country/region level. The position serves as the primary point of contact for investigative sites, coordinating documentation and timelines to enable study start-up. It involves working closely with project teams and external sites to keep activation processes moving in compliance with applicable regulations and SOPs.

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Required Skills

  • Site Activation
  • Feasibility
  • Regulatory Documentation
  • IRB Submission
  • Site Contracts
  • Document Review
  • Site Start-Up
  • Clinical Trials
  • Site Communications
  • Project Tracking

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IQVIA

About IQVIA

iqvia.com

IQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.

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