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Online Resumes with "ICH "
Clinical Trial Specialist / CRA _ Home based
Achieve the successful of clinical trial and ensure the subject safety and the high data quality by working closely with each clinical site and ensure that all the tasks are being conducted in accordance with the clinical trial protocol , ICH GCP guidelines and local regulations.
Clinical Trials Manager
Dear Hiring Manager, I am interested in exploring career opportunities with your company and have therefore enclosed my resume for your review. This position seems ideal for my experience, education, skills, and career interests. I am eager to contribute my enthusiasm and teamwork to your organization. My professional goal is to enhance my research development and senior leadership experience. I believe that I could...
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 document...
Tags for this Online Resume: Clinical Research Coordinator, Data Manager, Medical Assistant
