Clinical research administrator vs clinical trial coordinator

Differences between clinical research administrator and clinical trial coordinator duties and responsibilities

Clinical research administrator example responsibilities.

• Manage regional academic and community base oncology practices as the primary contact for all communications and support.
• Ensure effective data management and the following of good clinical practice (GCP) guidelines.
• Initiate the development of standard operating procedures for regulatory compliance monitoring and auditing of regulatory and IRB documentation.
• Assist with reports and documents to FDA.
• Train new site personnel on specific clinical trial procedures and appropriate FDA regulations.
• Develop and implement program for continual review and quality assessment of regulatory and IRB documentation.
Show more

Clinical trial coordinator example responsibilities.

• Establish and maintain strong community partnerships to achieve HIV prevention objectives.
• Coordinate grant and IRB renewals and submissions; and preparation of publications, study protocols and manuals of operations.
• Develop a GUI tool for volume & surface area of lesion/hematoma/edema in stroke MRI.
• Privilege to negotiation principles from the consumers stand point within the divisions of: oncology, bariatric, cosmetic & cardiovascular.
• Compose SPSS syntax to simplify data import process, reducing the time require from a full day to a few minutes.
• Analyze collected data using SPSS to determine possible significant findings.
Show more