Ray Cardello Email & Phone Number

United States

Ensure the smooth implementation of clinical trials, manage the clinical trial related personnel to complete the work according to the plan, manage the daily work of CRA, strengthen the project management, analyze. Deal with various problems encountered in the process to ensure the implementation progress. Develop the overall research plan of the clinical project according to the project timeline, and be responsible for the research screening of the clinical trial center. Project development and trial protocols. Case report form. Design the informed consent form and control the study progress and quality according to the key points. Organize various meetings such as protocol discussions and summary meetings according to the clinical trial progress

United States

Responsible for project management of clinical trials, quality control and schedule management, and conduct clinical trials in strict accordance with trial protocols, internal operational procedures and laws and regulations. Act as the main contact person for clinical trials and communicate important project related information and maintain good relationship with the commissioned research institutions and investigators on behalf of the company and project team

United States

Track clinical progress in related pharmaceutical fields according to the company's R&D strategy, collect and organize clinical research literature in related fields, provide clinical evaluation opinions for new products or new technology development, and develop clinical development plans for specific pipelines

United States

Develop clinical trial plans including clinical study design, clinical study protocol, informed consent, and clinical study report writing. Communicate with regulatory authorities regarding clinical trial medical related content

United States

Under the guidance of project managers and test engineers, prepare and improve the documentation used in clinical trials, complete the signing of clinical trial protocols, and follow up on the results of data audits. Assist in the completion of statistical analysis reports and clinical trial summary reports. Responsible for the collection of samples required for testing