Clinical Process Coordinator

Responsibility
• Complete appropriate role-specific training to perform job duties
• Under supervision, perform assigned administrative tasks to support team members with project execution (examples of such tasks include but not limited to running system reports, maintaining minutes of meeting, preparing and distributing status reports, creating and maintaining study documents, etc.)
• Under supervision, assist in updating and maintaining systems within project timelines and per project plans                                             

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
• Basic knowledge of applicable research and regulatory requirements, i.e., ICH GCP and relevant local laws, regulations and guidelines
• Exposure to MS Applications including but not limited to Microsoft Word, Excel and PowerPoint
• Effective written and verbal communication skills including good command of English language
• Effective time management skills
• Results and detail-oriented approach to work delivery and output
• Ability to establish and maintain effective working relationships with coworkers, managers and clients
• Strong listening and phone skills
• Good data entry skills

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 67,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.