Research Study Coordinator 2
University of Tennessee Athletic Marketing Department
Market Range: 10
Hiring Salary: $23.91/Hourly
THIS IS A TEMPORARY SIX-MONTH POSITION
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Department of Obstetrics and Gynecology is seeking a highly motivated and independent Research Study Coordinator 2. This position is ideal for individuals with a strong interest in women's health and clinical research, particularly those planning to apply to graduate health professional programs or residency training. The Research Study Coordinator 2 works closely with faculty and research teams to support ongoing clinical and health services research projects, with opportunities for mentorship, professional development, and clinical exposure.
Market Range: 10 Hiring Salary: $23.91/Hourly
MINIMUM REQUIREMENTS:
EDUCATION: Bachelor’s Degree. (TRANSCRIPT REQUIRED)
EXPERIENCE: Two (2) years of related work experience; OR a Master’s Degree will be accepted in lieu of experience; OR a combination of education and experience to equal six (6) years.
KNOWLEDGE, SKILLS, AND ABILITIES:
Ability to read and interpret scientific manuscripts and protocols.
Excellent written and verbal communication skills.
Strong organizational skills and attention to detail.
Ability to work independently and manage multiple projects simultaneously.
Knowledge of basic medical terms and how a health system operates.
Ability to be flexible with work hours to ensure that surgical specimens are collected timely.
WORK SCHEDULE: This position may occasionally be required to work evenings and weekends. May require occasional overnight travel.
Conducts weekly and daily screening of patients in the inpatient and outpatient settings to assess whether they meet study eligibility criteria.
Prepares consent forms, eligibility checklists, and other recruitment materials to bring to Labor and Delivery, Triage, or other various outpatient clinics with the purpose of consenting and enrolling patients.
Interacts with patients, nursing staff, and advance practice practitioners as part of the consenting and enrolling process.
Assists in the collection, processing, transport, and storage of biological specimens.
Writes and implements protocols, develops IRB applications, maintains eligibility checklists, surveys and questionnaires for research and human subjects’ projects.
Assist with regular record-keeping of enrollment numbers, protocol deviations, and adverse events.
Engages in literature reviews, data analysis, manuscript writing, and research presentations.
Assists with regular record-keeping of enrollment numbers, protocol deviations, and adverse events.
Conduct weekly or monthly study follow-ups (via email, virtual or in-person meetings) about each study to the principal investigator and other study personnel.
Performs other related duties as assigned.