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California Licensed Clinical Research Associate
A company is looking for a Clinical Research Associate (CRA) II. Key Responsibilities Conduct Phase I-IV clinical studies in compliance with Federal Regulations and ICH guidelines Assist in planning study conduct, including CRF design and CRO management Monitor investigational sites to ensure protocol adherence and timely patient enrollment Required Qualifications Experience in clinical research, specifically in Phase I-IV studies Knowledge of Federal Regulations and ICH guidelines Ability to manage and train investigator sites Experience in data management and CRF processing Contract employment availability
A company is looking for a Clinical Research Associate (CRA) II.
Key Responsibilities
Conduct Phase I-IV clinical studies in compliance with Federal Regulations and ICH guidelines
Assist in planning study conduct, including CRF design and CRO management
Monitor investigational sites to ensure protocol adherence and timely patient enrollment
Required Qualifications
Experience in clinical research, specifically in Phase I-IV studies
Knowledge of Federal Regulations and ICH guidelines
Ability to manage and train investigator sites
Experience in data management and CRF processing
Contract employment availability
