Site Monitoring Lead
IQVIA · Durham, NC
Clinical OperationsFull-time$93k–$233kCompany career page
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Role summary
IQVIA seeks a Site Management Lead to oversee clinical trial monitoring strategies and risk management at trial leadership level. This role requires developing risk-based monitoring approaches, training trial teams, and ensuring compliance with protocols and regulations across global studies from initiation through closeout.
What they're looking for
- Extensive end-to-end global clinical trial management experience through all phases
- Demonstrated expertise developing risk-based monitoring and risk management strategies
- Strong knowledge of site monitoring, site management processes, and ICH-GCP compliance
- Fluent English communication with ability to train CRAs and clinical trial managers
- University degree in life sciences or equivalent professional experience and knowledge
- Proficiency with centralized monitoring tools, dashboards, and data analytics
- Experience operating in complex international matrix organizational structures
What you'll be doing
- Author and maintain monitoring strategies, quality plans, and integrated risk management approaches
- Develop and deliver training on site monitoring topics to trial team members and investigators
- Oversee site monitoring activities and conduct oversight visits to ensure protocol adherence and compliance
- Perform continuous risk identification, data analysis, and issue escalation using centralized monitoring tools
- Lead trial-level issue management and communicate with regulatory authorities and ethics committees
Privacy & handoff
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