Margarita Gallardo

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• Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
• Maintained compliance with protocols covering patient care and clinical trial operations.
• Gathered, processed and shipped lab specimens.
• Exceeded goals through effective task prioritization and great work ethic.
• Worked within applicable standards, policies and regulatory guidelines to promote safe working environment.
• Carried out day-to-day duties accurately and efficiently.

Internal quality control manager
Responsible for external quality control Pacal and EQAS Unity

• Assisted with collecting, identifying and packaging hazardous and non-hazardous waste products to comply with Resource Conservation and Recovery Act regulations.
• Resolved routine issues and escalated non-standard or critical issues to department for corrective action.
• Cleaned and organized laboratory and kept supplies well-stocked to save time, money and promote laboratory efficiency.
• Repaired, calibrated and safely operated laboratory equipment to reduce costly instrument downtime.
• Established quality control measures for instrumentation and monitored data quality to operate instrument with control limits.
• Performed technical laboratory functions in compliance with regulatory agencies and safety requirements.
• Maintained organized, safe and efficient laboratory environment to minimize accidents and prevent cross contamination.
• Leveraged computerized management system and labeling process to conduct inventory of reagents, chemicals and supplies.

• Contributed to team discussions and new project initiatives to advance progress and optimize profitability.
• Assisted with collecting, identifying and packaging hazardous and non-hazardous waste products to comply with Resource Conservation and Recovery Act regulations.
• Repaired, calibrated and safely operated laboratory equipment to reduce costly instrument downtime.
• Resolved routine issues and escalated non-standard or critical issues to [Type] department for corrective action.

• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Participated in initiation visits and investigator meetings, implementing trials in accordance with study timelines and budgets.
• Gathered, processed and shipped lab specimens.
• Carried out day-to-day duties accurately and efficiently.
• Used Microsoft Word and other software tools to create documents and other communications.

• Maintained compliance with protocols covering patient care and clinical trial operations.
• Gathered, processed and shipped lab specimens.
• Devoted special emphasis to punctuality and worked to maintain outstanding attendance record.
• Carried out day-to-day duties accurately and efficiently.
• Used coordination and planning skills to achieve results according to schedule.
• Collaborated with team members to achieve target results.

• Performed technical laboratory functions in compliance with regulatory agencies and safety requirements.
• Monitored company inventory to keep stock levels and databases updated.

• Maintained excellent attendance record, consistently arriving to work on time.
• Developed and maintained courteous and effective working relationships.
• Learned new skills and applied to daily tasks to improve efficiency and productivity.
• Participated in team-building activities to enhance working relationships.
• Offered friendly and efficient service to customers, handled challenging situations with ease.
• Identified issues, analyzed information and provided solutions to problems.
• Carried out day-to-day duties accurately and efficiently.
• Worked to maintain outstanding attendance record, consistently arriving to work ready to start immediately.