Associate II, Field Clinical Monitoring - Aliso Viejo
2 weeks ago
Responsible for driving study execution and operational excellence in accordance with ICH Good Clinical Practices FDA regulations guidance documents and company SOPs.
+ Provide oversight of site compliance with study protocols informed consent procedures and data integrity requirements.
<+ Ensure accurate documentation timely reporting and consistent implementation of best practices.+ Identify develop and maintain investigators sites capable of delivering start-up goals enrollment targets required data quality.+ Facilitate maintain open communication among investigational sites study management teams key stakeholders.+ Work closely with Project Manager(s) to ensure clinical studies are conducted in accordance with the protocol GCP company SOPs applicable regulations.,
Job duties:
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- IDentify develop and maintain investigators sites capable of delivering start-up goals enrollment targets required data quality. ,
- Facilitate maintain open communication among investigational sites study management teams key stakeholders. ,
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Job description
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