The University of Tennessee Health Science Center
Research Study Coordinator- Research Center (Knoxville)
The University of Tennessee Health Science Center, Knoxville, Tennessee, United States, 37955
Research Study Coordinator- Research Center (Knoxville)
5 days ago Be among the first 25 applicants
Hiring Salary: $21.69/Hourly
Job Description Job Summary / Essential Job Functions:
The Research Study Coordinator for University of TN Knoxville- Graduate School of Medicine (UTK/GSM) assists the faculty with clinical research study activities including but not limited to the submission and management of regulatory paperwork, the submission of Institutional Review Board (IRB) applications and annual renewals, preparation and maintenance of study files and essential study documents. This position coordinates the operational and implementation of study protocols.
Responsibilities
Assists investigator with the execution and coordination of UTK/GSM collaborative Investigator-Initiated Clinical Research.
Assists UTK/GSM investigators with the design of studies by reviewing proposals to determine methods best suited to study objectives.
Assists investigators with the development and submission process for (IRB) approval including the collection of hospital collaboration agreements, key personnel documents, department approvals, funding source information, and IRB application completion.
Assists investigators with the development of data extraction sheets and the process of data extraction from Electronic Medical Records (EMR) or Investigator-Initiated Studies and assists in developing relational databases for tracking study subjects.
Assists investigator with the IRB process for protocol amendments and/or adding or removing IRB-approved personnel from an investigation-initiated project; assists faculty with the IRB process for the IRB Adverse Events, Serious Adverse Events, and Protocol Deviations.
Assists in screening potential subjects, reviewing and documenting patient medical histories and concurrent medication, obtaining informed consent, coordinating study visits and procedures to be completed on campus, collecting study data, and performing study assessments if needed (lab draws, questionnaires, vital signs, etc.) for Investigator-Initiated Studies.
Establishes and maintains contact with study participants and families, community agencies, and health care providers.
Assists investigator with the management and maintenance of study-specific Master Study Files and Essential Study Documents.
Assists with the management and maintenance of Subject Source Documents.
Facilitates study-specific communication and meetings.
Performs other duties as assigned.
Qualifications Education:
Bachelor’s Degree in a relevant health field.
(TRANSCRIPT REQUIRED)
Experience:
One (1) year of relevant experience; or Associate’s Degree and three (3) years of relevant experience; or an equivalent combination of education, training, and experience to equal five (5) years.
Knowledge, Skills, And Abilities
Ability to create and maintain extensive medical records on clinical research subjects.
Understanding of hospital policies and procedures, medical records and documentation, and HIPAA regulations.
Knowledge of research protocol with an understanding of Basic Research Principles and the Federal Code of Regulations for Clinical Research Studies.
Ability to manage multiple priorities.
Intermediate-level computer skills with the ability to learn new software applications for various electronic data capture programs.
Understanding complex diagnoses and procedures.
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Higher Education
Referrals increase your chances of interviewing at The University of Tennessee Health Science Center by 2x
Get notified about new Research Study Coordinator jobs in Knoxville, TN.
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Hiring Salary: $21.69/Hourly
Job Description Job Summary / Essential Job Functions:
The Research Study Coordinator for University of TN Knoxville- Graduate School of Medicine (UTK/GSM) assists the faculty with clinical research study activities including but not limited to the submission and management of regulatory paperwork, the submission of Institutional Review Board (IRB) applications and annual renewals, preparation and maintenance of study files and essential study documents. This position coordinates the operational and implementation of study protocols.
Responsibilities
Assists investigator with the execution and coordination of UTK/GSM collaborative Investigator-Initiated Clinical Research.
Assists UTK/GSM investigators with the design of studies by reviewing proposals to determine methods best suited to study objectives.
Assists investigators with the development and submission process for (IRB) approval including the collection of hospital collaboration agreements, key personnel documents, department approvals, funding source information, and IRB application completion.
Assists investigators with the development of data extraction sheets and the process of data extraction from Electronic Medical Records (EMR) or Investigator-Initiated Studies and assists in developing relational databases for tracking study subjects.
Assists investigator with the IRB process for protocol amendments and/or adding or removing IRB-approved personnel from an investigation-initiated project; assists faculty with the IRB process for the IRB Adverse Events, Serious Adverse Events, and Protocol Deviations.
Assists in screening potential subjects, reviewing and documenting patient medical histories and concurrent medication, obtaining informed consent, coordinating study visits and procedures to be completed on campus, collecting study data, and performing study assessments if needed (lab draws, questionnaires, vital signs, etc.) for Investigator-Initiated Studies.
Establishes and maintains contact with study participants and families, community agencies, and health care providers.
Assists investigator with the management and maintenance of study-specific Master Study Files and Essential Study Documents.
Assists with the management and maintenance of Subject Source Documents.
Facilitates study-specific communication and meetings.
Performs other duties as assigned.
Qualifications Education:
Bachelor’s Degree in a relevant health field.
(TRANSCRIPT REQUIRED)
Experience:
One (1) year of relevant experience; or Associate’s Degree and three (3) years of relevant experience; or an equivalent combination of education, training, and experience to equal five (5) years.
Knowledge, Skills, And Abilities
Ability to create and maintain extensive medical records on clinical research subjects.
Understanding of hospital policies and procedures, medical records and documentation, and HIPAA regulations.
Knowledge of research protocol with an understanding of Basic Research Principles and the Federal Code of Regulations for Clinical Research Studies.
Ability to manage multiple priorities.
Intermediate-level computer skills with the ability to learn new software applications for various electronic data capture programs.
Understanding complex diagnoses and procedures.
Seniority level
Entry level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Higher Education
Referrals increase your chances of interviewing at The University of Tennessee Health Science Center by 2x
Get notified about new Research Study Coordinator jobs in Knoxville, TN.
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr