RSU Specialist I, FSP Sponsor Dedicated
IQVIA · Mexico City, Mexico
Clinical OperationsFull-timeCompany career page
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Role summary
IQVIA seeks a Regulatory & Start Up Specialist to serve as the primary contact for assigned clinical studies and sites in Mexico, managing study activation, regulatory documentation, and project timelines in a fully remote role.
What they're looking for
- Bachelor's degree in life sciences
- Minimum 1 year clinical research and study start-up management experience
- Fluent English written and oral communication
- Analytical and critical thinking skills with multi-perspective evaluation ability
- Strong interpersonal skills with adaptability to changing requirements
- Demonstrated ability managing multiple priorities in fast-paced environments
What you'll be doing
- Serve as single point of contact for assigned studies, sites, and internal teams
- Execute site activation and regulatory document preparation per SOPs and regulations
- Maintain internal systems, databases, and tracking tools with accurate project information
- Monitor site performance metrics and provide feedback to management
- Track and follow up on regulatory, ethics, and document approvals against project timelines
Privacy & handoff
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