Tracey Diaz Email & Phone Number

Oakley, Ca, Us

• Receive and inventory all shipments of clinical laboratory and GLP study samples.• Document abnormalities upon receipt and communicate with investigational site and/or clinical site staff to resolve abnormalities. • Perform over-labeling of specimens as necessary.• Enter sample information and maintain database records, reports and paperwork to ensure cGCP, (Good Clinical Practices), standards are maintained.• Transfer/Ship samples to appropriate groups for analysis and maintain chain of custody paperwork.• Archive or dispose of samples.• Coordinate validation samples and maintain database records.• Create clinical data collection forms and sample container labels to support clinical studies.• Support the GLP label station and other database front ends.• Coordinate labeling, secondary packaging, and shipping functions to meet pre-clinical demands.• Create and maintain Standard Operating Procedures (SOPs).• Monitor sample storage freezers, including daily monitoring, changing chart recorders, repair logs, and cleaning.• Member of company’s Emergency Response Team, 2005 to 2009

• Schedule appointments for CNA testing. Administer and grade tests, and set up appointments with recruiters.• Schedule appointments for recruiters for various other positions, and enter applicant information into data tracking system. • Assist with preparation of documents for recruiting seminars.• Organize and file miscellaneous HR documentation.• Post weekly printouts of job openings.

• Receive and inventory all shipments of clinical laboratory and GLP study samples.• Document abnormalities upon receipt and communicate with investigational site and/or clinical site staff to resolve abnormalities. Perform over-labeling as necessary.• Enter sample information and maintain database records, reports and paperwork to ensure cGCP, (Good Clinical Practices), standards are maintained.• Transfer/Ship samples to appropriate groups for analysis and maintain chain of custody paperwork.• Archive or dispose of samples.• Coordinate validation samples and maintain database records.• Create clinical data collection forms and sample container labels to support clinical studies.• Support the GLP label station and other database front ends.• Coordinate labeling, secondary packaging, and shipping functions to meet pre-clinical demands.• Create and maintain Standard Operating Procedures (SOPs).• Monitor sample storage freezers, including daily monitoring, changing chart recorders, repair logs, and cleaning.• Volunteered for two years as Laboratory Representative to Sample Management Group• Member of company’s Emergency Response Team, 2003 to 2004• Joined Cerus as Clinical Samples Coordinator in September 2000; promoted to Coordinator II in March 2001, and Coordinator III in March 2004.

• Support proprietary software serving the pharmaceutical industry in the process of conducting clinical trials. Provided general support for supplemental software.• Assisted investigator sites from inception of clinical trial studies to completion.• Configured MS DOS based and Windows based systems and also provided hardware support.• Assisted with training preparation and provided client/site training as required.• Maintained all documentation for daily support and change control activities.• Performed repair procedures for client data and flag files associated with proprietary software.• Responsible for client software upgrades and mid-study changes and all associated documentation.• Assisted with writing and maintaining Standard Operating Procedures (SOPs).• Generated client reports.• Joined MiniDoc as Support Assistant in 1993; promoted to Support Specialist in 1995 and to Senior Support Specialist in 1997.