Job Description:

ResponsibilitiesTo collect and record preliminary data for clinical research programsTo recruit and perform follow-up with research participants as protocols outlineTo schedule visits according to research protocolsTo assist in coordination of lab and fieldworkTo maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulationsPrepares for study monitoring visitsAssists with correcting findingsAssists with the completion of Case Report Forms (CRF) according to protocolAssists with development of protocols and standard operating procedures (SOPs) for data quality assurancePerforms general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study suppliesmaterials)May perform a variety of medical procedures under supervisionMay assist in compiling, editing, and proofing written reports for both internal and external administrative officesMay perform data analysis using a variety of software packagesUses Electronic Data Capture (EDC) systems necessary for operations under supervisionPerforms other duties as assignedKey Duties & Responsibilities Collects and records preliminary data for clinical research programs. Recruits and performs follow-up with research participants as protocols outline. Schedules visits according to research protocols. Assists in coordination of lab and fieldwork. Prepares for study monitoring visits. Assists with correcting findings. Assists with the completion of Case Report Forms (CRF) according to protocol. Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance. Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study suppliesmaterials).May perform a variety of medical procedures under supervision.May assist in compiling, editing, and proofing written reports for both internal and external administrative offices. May perform data analysis using a variety of software packages. Uses Electronic Data Capture (EDC) systems necessary for operations under supervisionPerforms other duties as assigned.QualificationsHigh School diploma or GED requiredPrefer candidates with a bachelor's and two (2) years' experience working in a clinical settingKnowledge of clinical trial processes, data collection, data entryExperience with recruiting and performing follow-up with research participants as protocols outlineKnowledge of protocols and standard operating procedures (SOPs) for data quality assuranceFace-to-face patient communication experience