Skip to main content
Tallo logoTallo logo
Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Research Study Coordinator 2-Obstetrics and Gynecology

Job

University of Tennessee - Knoxville

Memphis, TN (In Person)

$55,675 Salary, Full-Time

Posted 3 weeks ago (Updated 2 weeks ago) • Actively hiring

Expires 6/29/2026

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
84
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Research Study Coordinator 2-Obstetrics and Gynecology University of Tennessee - Knoxville - 4.1 Memphis, TN Job Details Full-time $4,182.12 - $5,000.00 a month 1 day ago Qualifications Anatomy knowledge Bachelor's degree Medical terminology
Technical Proficiency Full Job Description Market Range:
10
Hiring Salary:
$4,182.12 - $5,000.00/Monthly
THIS IS A GRANT-FUNDED POSITION FUNDED UNTIL JULY 1, 2027. THE FUNDING MAY BE EXTENDED PENDING FUNDING AVAILABILITY. JOB SUMMARY/ESSENTIAL JOB FUNCTIONS
The Research Study Coordinator 2 plans, directs, and coordinates activities related to clinical research in the Department of Obstetrics & Gynecology. This position is responsible for understanding research protocols and regulatory guidelines and accurately completing research tasks in order to achieve the goals of the projects and the department. Submits new protocols for institutional approval bodies and observes reporting requirements of these bodies throughout the study. Assists in study planning and development, including protocol development, creating study forms, and mediating budget and contract communications. Conducts and documents surveys, patient interviews, or observational data per protocol requirements. Creates and maintains study logs for effective trial management; maintains regulatory documents and study communications in the appropriate projects critical documents binder. Coordinates daily study activities and communicates with study personnel to ensure adequate staff coverage for protocol and regulatory requirements Learns the protocols and procedures of each study as assigned and be prepared to perform delegated duties as required by the protocol Monitors and documents adverse events, protocol deviations, and barriers to success. Trains clinical or research staff to specific research protocols as indicated or assigned. Performs or assists with the collection, documentation, processing and shipping of lab samples Abstracts patient health information for entry into research data collection forms. Completes required training certificatio ns (CITI, IATA, lab safety, etc.) and comply to relevant guidelines Performs other duties as assigned.
MINIMUM REQUIREMENTS
EDUCATION:
Bachelor's Degree. (TRANSCRIPT
REQUIRED
)
EXPERIENCE
Two (2) years related experience; OR a combination of education and experience to equal six (6) years.
KNOWLEDGE, SKILLS, AND ABILITIES
Ability to communicate and collaborate in a professionally. Excellent reading comprehension. Excellent time management. Knowledge of medical terminology, anatomy, and physiology. Proficient computer skills and readiness to learn new software and equipment. Accuracy and attention to detail.
WORK SCHEDULE
This position may occasionally be required to work weekends and evenings. May require occasional overnight travel.