SiteActivationCoordinator

**Site Activation Coordinator** **Country Site Activation – CSA** **Entry-Level & Senior Opportunities Available** **South Africa** **Shape the Future of Patient Health** At IQVIA, we’re united by one mission: **to improve patient outcomes around the world**. Our Global Site Activation community—over 2,000 strong—plays a critical role in bringing clinical trials to life. By activating sites efficiently, accurately, and with exceptional quality, we help ensure patients gain access to safe, effective, and innovative treatments. Our focus is simple: **Always Impatient for the Patient.** And we’re looking for people who share that passion. **About the Role** We’re recruiting for **both Entry-Level and Senior Site Activation Coordinator positions**. Your level will be determined based on your experience, capability, and career trajectory. As a Site Activation Coordinator, you will support essential country-level activities that enable clinical trial sites to begin operations. You’ll collaborate with cross‑functional teams, manage study documentation, ensure compliance, and help drive the timely activation of investigative sites. This is a great opportunity to build or accelerate your career in clinical research within a global, innovative environment. **What You’ll Be Doing** * Support feasibility assessments, site activation tasks, and selected maintenance activities for assigned studies. * Work closely with Site Activation Managers, Project Management teams, and other internal stakeholders. * Prepare, review, track, and follow up on essential study documentation, including: * Feasibility questionnaires * CDAs * Regulatory and ethics submissions * Informed Consent Forms * Investigator Pack documentation * Review documents for completeness, consistency, and accuracy. * Maintain accurate and up-to-date information across internal systems, trackers, databases, and project plans. * Ensure activities are conducted in accordance with local regulations, global SOPs, and study