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Clinical Research Coordinator New Orleans, LA
Monitor assigned clinical trials, interact with all different department such as (monitoring resources, project manager, quality assurance and data management). Conduct site visits (initiation, monitoring and close out). Ensure the adherence to FDA, ICH & GCP regulations. Instruct the site staff in their roles and responsibilities in conducting clinical trials. Ensure the completion and collection of regulatory documents, evaluate and report site performance and protocol compliance. Ensure completion and collection of SAE's, assist with data valation resolution of queries.
Analyst
About Me
Industry: |
Research |
|---|---|
Occupation: |
Analyst |
Education level: |
Bachelor |
Will Relocate: |
Yes |
Location: |
Marrero, LA |
