What are the responsibilities and job description for the Research Data Coordinator-Research Center Part-Time (Knoxville) position at University of Tennessee, Knoxville?
Market Range: 10
Hiring Salary: $23.91/Hourly
THIS IS A PART-TIME POSITION (20 HOURS PER WEEK)
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under the direction of the GSM Director of Research, the Research Data Coordinator is responsible for the management of clinical research study data and specific databases for Investigator-Initiated Research. This position develops Patient Source and EMR Extraction Documents for retrospective and prospective Investigator-Initiated research, transcribes data into appropriate databases, conducts routine data analysis on collected data and reviews data for discrepancies, queries generation, resolution, and reconciliation, and write-up data findings.
Duties And Responsibilities
Generates study-specific source documents and data-extraction sheets for Investigator-Initiated Research.
EDUCATION: Bachelor’s Degree in relevant health-field. (Master’s Degree in Public Health or health related field preferred.) (TRANSCRIPT REQUIRED)
EXPERIENCE: Two (2) years of related experience; OR a combination of college coursework and related work experience to equal six (6) years.
Knowledge, Skills, And Abilities
Other Professional
Primary Location
US-Tennessee-knoxville
Organization
Knox Research - No Longer Used
Schedule
Part-time
Campus/Institute
Memphis
Job Posting
Nov 25, 2024, 2:58:02 PM
Hiring Salary: $23.91/Hourly
THIS IS A PART-TIME POSITION (20 HOURS PER WEEK)
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under the direction of the GSM Director of Research, the Research Data Coordinator is responsible for the management of clinical research study data and specific databases for Investigator-Initiated Research. This position develops Patient Source and EMR Extraction Documents for retrospective and prospective Investigator-Initiated research, transcribes data into appropriate databases, conducts routine data analysis on collected data and reviews data for discrepancies, queries generation, resolution, and reconciliation, and write-up data findings.
Duties And Responsibilities
Generates study-specific source documents and data-extraction sheets for Investigator-Initiated Research.
- Coordinates the development of Redcap and/or Excel databases for Investigator-Initiated Research.
- Completes data entry into Electronic Data Capture Systems (EDC) for study-specific Investigator-Initiated protocols.
- Assists local team members and department research coordinator with administrative activities including the storing and management of study data during study conduct and post-study closure.
- Assists Research Coordinator with IRB Continuing Review processes that include the completion of study status reports, demographic percentages, safety reports, deviation reports, new findings related to study interventions and uploads into iMedRIS for departmental research projects.
- Assists Faculty and Investigators with abstract and manuscript development and submission post-data collection for Investigator-Initiated Research.
- Performs routine data analysis and provides essential information to the GSM Office of Biostatistics Director and/or designee during the Data Analysis phase of Investigator-Initiated Research.
- Assists faculty with the identification of potential funding opportunities and works with study teams to generate grant documents for submission.
- Identifies appropriate journals for Investigator-Initiated Research findings submission.
- Performs other duties as assigned.
EDUCATION: Bachelor’s Degree in relevant health-field. (Master’s Degree in Public Health or health related field preferred.) (TRANSCRIPT REQUIRED)
EXPERIENCE: Two (2) years of related experience; OR a combination of college coursework and related work experience to equal six (6) years.
Knowledge, Skills, And Abilities
- Ability to create and maintain extensive medical records on clinical research subjects.
- An understanding of complex diagnoses, medications, and procedures.
- Understanding of Basic Research Principles and Federal Code of Regulations for Clinical Research Studies.
- Understanding of hospital policies and procedures, medical records and documentation, and HIPPA regulations
- Knowledge of research protocols
- Interpersonal and communication skills.
- Highly developed planning and organizing skills.
- Ability to manage multiple priorities.
- Ability to work with diverse populations.
- Intermediate level computer skills with the ability to learn new software applications for various electronic data capture programs
Other Professional
Primary Location
US-Tennessee-knoxville
Organization
Knox Research - No Longer Used
Schedule
Part-time
Campus/Institute
Memphis
Job Posting
Nov 25, 2024, 2:58:02 PM
Salary : $24
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