Related skills
cro veeva etmf ctms ich-gcpπ Description
- Lead scalable clinical ops for multi-site trials across programs
- Establish standardized site startup, monitoring, enrollment, and oversight processes
- Define KPIs and dashboards to monitor study health and performance
- Develop systems to ensure inspection-ready execution across studies
- Oversee site operations, monitoring, and vendor/CRO performance
- Ensure adherence to ICH-GCP and regulatory standards
π― Requirements
- Bachelor's degree in scientific field; advanced degree preferred
- 10+ years in progressive clinical operations roles, preferably diagnostics
- 6+ years of people leadership across multiple roles
- Experience building scaling clinical ops infrastructure, processes
- Experience with Medrio (EDC), CTMS and eTMF systems; Veeva preferred
- Strong cross-functional collaboration and program management
π Benefits
- Opportunity to work on cutting-edge infectious disease diagnostics
- Travel up to 10% as needed
- Hybrid remote options and flexible work environment
- Strong, collaborative team culture
- Competitive compensation and equity package
- Equal opportunity employer with inclusive culture
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