• Coordinate data collection by interviewing subjects, collecting vitals, and reporting adverse events and concomitant medications in compliance with federal regulations.• Organize recruitment, education, and scheduling of participating patients in compliance with independent review boards.• Responsible for accurate, detailed electronic data capture and resolution of data queries within a timely manner using various platforms.• Perform quality control by reviewing data for… Show more • Coordinate data collection by interviewing subjects, collecting vitals, and reporting adverse events and concomitant medications in compliance with federal regulations.• Organize recruitment, education, and scheduling of participating patients in compliance with independent review boards.• Responsible for accurate, detailed electronic data capture and resolution of data queries within a timely manner using various platforms.• Perform quality control by reviewing data for discrepancies and reporting and correcting discrepancies • Interface with sponsoring pharmaceutical companies, contract research organizations, independent review boards, and laboratories.• Manage the processing and shipping of human biological specimens for clinical trials in compliance with IATA regulations.• Facilitate the ordering, tracking, storing, inspecting, and documenting of experimental products and clinical test equipment. Show less

• Process and ship human biological specimens for clinical trials under the International Air Transport Association (IATA) regulations• Create original, detailed source documents for data capture as well as revising existing source documents • Maintain and update inventory by ordering, receiving, and storing experimental drug and other study supplies• Responsible for detailed electronic data capture (EDC) entry and resolution of data queries within a timely manner• Perform… Show more • Process and ship human biological specimens for clinical trials under the International Air Transport Association (IATA) regulations• Create original, detailed source documents for data capture as well as revising existing source documents • Maintain and update inventory by ordering, receiving, and storing experimental drug and other study supplies• Responsible for detailed electronic data capture (EDC) entry and resolution of data queries within a timely manner• Perform quality control by analyzing data for errors and reporting errors when they arise• Maintain enrollment logs, investigational product logs, and subject identification logs. • Support with the clinical and administrative tasks throughout numerous clinical trials • Practice GCP, HIPPA, and OSHA standards• Handle phone, mail, and email correspondence and relay messages when appropriate• Recruit, educate, and schedule subjects for research studies within study-specific time frames• Retrieve confidential medical records Show less

• Process applications by submitting background checks and motor vehicle reports• Maintain physical and electronic employee files• Advertise job openings as needed to sustain workflow• Perform quality control by analyzing data for errors and reporting errors when they arise

• Process and ship human biological specimens for clinical trials under the International Air Transport Association (IATA) regulations• Create original, detailed source documents for data capture as well as revising existing source documents • Assist in completing SIVs, COVs, and interim monitoring visits• Maintain and update inventory by ordering, receiving, and storing experimental drug and other study supplies• Responsible for detailed electronic data capture (EDC) entry and… Show more • Process and ship human biological specimens for clinical trials under the International Air Transport Association (IATA) regulations• Create original, detailed source documents for data capture as well as revising existing source documents • Assist in completing SIVs, COVs, and interim monitoring visits• Maintain and update inventory by ordering, receiving, and storing experimental drug and other study supplies• Responsible for detailed electronic data capture (EDC) entry and resolution of data queries within a timely manner• Perform quality control by analyzing data for errors and reporting errors when they arise• Maintain enrollment logs, investigational product logs, and subject identification logs. • Support with the clinical and administrative tasks throughout numerous clinical trials • Practice GCP, HIPPA, and OSHA standards• Handle phone, mail, and email correspondence and relay messages when appropriate• Recruit, educate, and schedule subjects for research studies within study-specific time frames• Retrieve confidential medical records• Assist in archiving past clinical trial materials Show less