Purpose and Scope of Position Duties and Responsibilities Job Requirements This position works with the Clinical Sites Director and helps to support, facilitate, and coordinate all daily study program activities and plays a critical role in the data entry of the study program. Specific Job Duties/Responsibilities Training Assist with the study program objectives and monitor quantitative and qualitative data on progress towards objectives. Review objectives to identify problems and solutions, prioritize solutions and develop action steps for program implement. Compile statistics of assessment/evaluation questionnaires and prepare analysis reports. Learn internal systems for data collection and submission. Perform related duties based on the departmental need and other duties as requested by Regenative Labs Management. Employee will be trained on proper data collection methods by clinical research coordinators. Employee will complete Good Clinical Practice, Protecting Human Research Participants, FDA HCT/P, and HIPAA certifications during the initial training period. Certifications will be collected and filed. Education/Credentials Experience & Training Technical Requirements/Skills Working Conditions BA/BS degree from an accredited college or university is preferred. High school diploma or General Education Degree is required. Must be proficient in Microsoft Excel Must be able to reason independently and work with minimal guidance. Must be able to adapt quickly to changing priorities and schedules. Ability to maintain good working relationships with all co-workers and the public. PC Literate will be utilized (Word, Access, Excel, etc.)
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