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Clinical Research Coordinator-Infectious Diseases-Jackson Medical Mall

University of Mississippi Medical Center

Jackson, MSFull-timePosted 1w agoStill listed today

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At a glance

Compensation
No compensation found
Location
Jackson, MS
Schedule
Full-time
Work Authorization
Not specified

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Requirements

Credentials this posting asks for.

Bachelor's degree, required

Job overview

The Clinical Research Coordinator manages and reports clinical study results, coordinates research activities, supervises the research team, and directs participant enrollment while maintaining study-record integrity. The role also prepares grant progress documentation and monitors budgets. Prior clinical trial research experience is preferred. The position requires a bachelor's degree and two years of research administration or support experience.

Skills & qualifications

RequiredNice to have

Skills

Good Clinical Practice, requiredFDA Regulations, requiredOral Communication, requiredWritten Communication, requiredInterpersonal Skills, requiredComputer Systems, requiredComputer Tools, requiredComputer Programs, requiredTeam Leadership, requiredIRB Submissions, requiredPatient Screening, requiredPatient Consenting, requiredOrganizational Skills, requiredClinical Trial Research, nice to have

Qualifications

Bachelor's Degree, required2 Years Research Administration or Support Experience, required

Full job description

Hello,

Thank you for your interest in career opportunities with the University of Mississippi Medical Center. Please review the following instructions prior to submitting your job application:

  • Provide all of your employment history, education, and licenses/certifications/registrations. You will be unable to modify your application after you have submitted it.
  • You must meet all of the job requirements at the time of submitting the application.
  • You can only apply one time to a job requisition.
  • Once you start the application process you cannot save your work. Please ensure you have all required attachment(s) available to complete your application before you begin the process.
  • Applications must be submitted prior to the close of the recruitment. Once recruitment has closed, applications will no longer be accepted.

After you apply, we will review your qualifications and contact you if your application is among the most highly qualified. Due to the large volume of applications, we are unable to individually respond to all applicants. You may check the status of your application via your Candidate Profile.

Thank you, Human Resources

Important Applications Instructions:

Please complete this application in entirety by providing all of your work experience, education and certifications/ license. You will be unable to edit/add/change your application once it is submitted.

Job Requisition ID: R00053948

Job Category: Research

Organization: SOM-Medicine-ID - PI II

Location/s: Jackson Medical Mall

Job Title: Clinical Research Coordinator-Infectious Diseases-Jackson Medical Mall

Job Summary: Responsible for management, execution, and reporting of clinical study results and the supervision of the research team. Coordinates activities for research studies within an assigned area or unit. Directs participant enrollment in research studies and assures integrity of study records. Prepares and submits documentation for institutional and governmental grant progress review and budget monitoring.

Education & Experience Education and Experience Required: Bachelor's Degree and two (2) years of research administration or support experience.

Certifications, Licenses or Registration Required: N/A

Preferred Qualifications: Prior experience in clinical trial research is preferred.

Knowledge, Skills & Abilities Knowledge, Skills, and Abilities: Excellent knowledge of good clinical practice and FDA regulations. Superior oral and written communication skills. Strong interpersonal skills to effectively interact with patients, physicians, staff, and study sponsors. Knowledge and understanding of computer systems, tools, and programs. Ability to assume a leadership role in a team environment. Working knowledge of IRB submissions/amendments, patient screening and consenting. Excellent organizational skills.

Responsibilities:

  • Assumes responsibility for all aspects of study recruitment, screening, enrollment, and visits for eligible participants. Administers study-related procedures & instruments; directs participants for hospital and physician procedures.
  • Ensures that research personnel are knowledgeable about all components of the study protocol and that staff roles and responsibilities are delineated.
  • Oversees and manages scheduling, documentation, and follow-ups with research participants. Supervises patient education and referrals.
  • Monitors study budgets and billings to insure adequacy of funds and compliance with UMMC policies and federal regulations.
  • Corresponds with study investigators, sponsors, regulatory agencies, and UMMC compliance personnel on matters related to study documentation, records, data and operations.
  • Prepares IRB documents and progress reports. Oversees maintenance of regulatory documents, files, and reports.
  • The duties listed are general in nature and are examples of the duties and responsibilities performed and are not meant to be construed as exclusive or all-inclusive. Management retains the right to add or change duties at any time.

Physical and Environmental Demands Requires frequent exposure to unpleasant or disagreeable physical environment such as high noise level and exposure to heat and cold, frequent handling or working with potentially dangerous equipment, frequent exposure to bio-hazardous conditions such as risk of radiation exposure, blood borne pathogens, fumes or airborne particles, and/or toxic or caustic chemicals which mandate attention to safety considerations, occasional working hours significantly beyond regularly scheduled hours, occasional travelling to offsite locations, occasional activities subject to significant volume changes of a seasonal/clinical nature, occasional work produced subject to precise measures of quantity and quality, frequent bending, occasional lifting and carrying up to 50 pounds, frequent crouching/stooping, occasional driving, occasional kneeling, frequent pushing/pulling, frequent reaching, frequent sitting, frequent standing, frequent twisting, and frequent walking. (occasional-up to 20%, frequent-from 21% to 50%, constant-51% or more)

Time Type: Full time

FLSA Designation/Job Exempt: Yes

Pay Class: Salary

FTE %: 100

Work Shift: Day

Benefits Eligibility:

Grant Funded: Yes

Job Posting Date: 10/28/2026

Job Closing Date (open until filled if no date specified):

How this job compares

Set against the 624 open Clinical Research Coordinator jobs on Olive Jobs, counted November 10, 2026.

Pay
  • This postingNot listed
  • US median$56–74K/yr152 salary ranges
  • US median$24–36/hr197 hourly ranges
Openings
Olive Jobs lists 624 open Clinical Research Coordinator jobs across the US. 2% of them nationwide are listed as remote or flexible.
Hiring the most across the US
Experience
This posting asks for at least 2 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (408 postings).
Education
This posting asks for a bachelor's degree; 186 of the 624 open Clinical Research Coordinator jobs (30%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 10, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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