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Creative Clinical Research Associate with extensive project experience from concept to development. Talents include in-depth knowledge of ICH guidelines, SAE reporting, and GCP auditing. Integral team player with excellent communication skills; fluent in French.
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- Monitor subject follow-up from 3-year clinical trial.
- Coordinate laboratory samples and compile data.
- Collaborate with medical professionals to determine changes in subjects’ conditions.
- Managed Geo-nix project and oversaw team of 4 Research Associates.
- Maintained SOPs and Good Clinical Practice in compliance with ICH guidelines.
- Scheduled and led team study meetings; reported findings to Lead CRA.
- Screened and recruited subjects based on eligibility criteria for project participation.
- Served as point of contact for Clinical Research Professionals.
- Conducted pre-site visits and performed site evaluations.
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