ZipRecruiter

Log In

1

Clinical Study Coordinator Jobs in Oak Ridge, TN

Tennessee Oncology

Clinical Trial Specialist

Midtown, TN · On-site

... coordinating activities associated with clinical trials under the mentorship and guidance of a ... Manage and lead cross-functional study teams, including vendors; liaise with other functional areas ...

Covenant Health

Clin Research Nurse Coord

Knoxville, TN · On-site

$65K - $82K/yr

Plans and implements pre-study activities by developing timelines for conducting the clinical trial ... Coordinates patient enrollment in clinical trials by following randomization procedures as per ...

Covenant Health

Clin Research Nurse Coord

Knoxville, TN

$65K - $82K/yr

Plans and implements pre-study activities by developing timelines for conducting the clinical trial ... Coordinates patient enrollment in clinical trials by following randomization procedures as per ...

Elevance Health

LTSS Service Coordinator

Knoxville, TN · On-site

$18.75 - $23.75/hr

Manages non-clinical needs of members with chronic illnesses, co-morbidities, and/or disabilities ... BA/BS degree field of study in health care related field preferred. * Travels to worksite and other ...

Elevance Health

LTSS Service Coordinator

Knoxville, TN · On-site

$18.75 - $23.75/hr

Manages non-clinical needs of members with chronic illnesses, co-morbidities, and/or disabilities ... BA/BS degree field of study in health care related field preferred. * Travels to worksite and other ...

Elevance Health

LTSS Service Coordinator

Kingston, TN · On-site

$17 - $21.50/hr

Manages non-clinical needs of members with chronic illnesses, co-morbidities, and/or disabilities ... BA/BS degree field of study in health care related field preferred. * Travels to worksite and other ...

Elevance Health

LTSS Service Coordinator

Kingston, TN · Hybrid

$17 - $21.50/hr

Manages non-clinical needs of members with chronic illnesses, co-morbidities, and/or disabilities ... BA/BS degree field of study in health care related field preferred. * Travels to worksite and other ...

Elevance Health

LTSS Service Coordinator

Kingston, TN · Hybrid

$17 - $21.50/hr

Manages non-clinical needs of members with chronic illnesses, co-morbidities, and/or disabilities ... BA/BS degree field of study in health care related field preferred. * Travels to worksite and other ...

Elevance Health

LTSS Service Coordinator

Knoxville, TN · Hybrid

$18.75 - $23.75/hr

Manages non-clinical needs of members with chronic illnesses, co-morbidities, and/or disabilities ... BA/BS degree field of study in health care related field preferred. * Travels to worksite and other ...

Elevance Health

LTSS Service Coordinator

Knoxville, TN · Hybrid

$18.75 - $23.75/hr

Manages non-clinical needs of members with chronic illnesses, co-morbidities, and/or disabilities ... BA/BS degree field of study in health care related field preferred. * Travels to worksite and other ...

Elevance Health

LTSS Service Coordinator

Maryville, TN · Hybrid

$17.25 - $21.75/hr

Manages non-clinical needs of members with chronic illnesses, co-morbidities, and/or disabilities ... BA/BS degree field of study in health care related field preferred. * Travels to worksite and other ...

next page

Showing results 1-20

All JobsClinical Study JobsClinical Study Coordinator JobsClinical Study Coordinator Jobs in Oak Ridge, TN

Clinical Study Coordinator information

See Oak Ridge, TN salary details

$26.8K

$64.6K

$110.9K

How much do clinical study coordinator jobs pay per year?

As of Sep 2, 2026, the average yearly pay for clinical study coordinator in Oak Ridge, TN is $64,573.00, according to ZipRecruiter salary data. Most workers in this role earn between $51,100.00 and $75,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study coordinator?

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, often supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, IRB submission processes, and Good Clinical Practice (GCP) certification is highly valued. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating study teams and liaising with stakeholders. These abilities ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, safeguarding both data integrity and participant safety.

What are some common challenges clinical study coordinators face when managing multiple studies at once?

Clinical Study Coordinators often juggle several studies simultaneously, which requires strong organizational and time-management skills. Challenges include prioritizing tasks, ensuring regulatory compliance across different protocols, and keeping accurate documentation for each study. Effective communication with investigators, sponsors, and participants is essential to prevent misunderstandings and maintain study timelines. Utilizing project management tools and maintaining up-to-date records can help coordinators stay on track and reduce stress.

What is the difference between Clinical Study Coordinator vs Clinical Research Associate?

AspectClinical Study CoordinatorClinical Research Associate
Required CredentialsTypically a bachelor's degree in health sciences or related field; certifications like CCRP are a plusOften a bachelor's degree in life sciences; certifications like CCRP or RAC are common
Work EnvironmentConducts site visits, manages study activities at clinical sitesMonitors multiple sites remotely or on-site, ensuring protocol compliance
Employer & Industry UsageHospitals, clinics, research sitesPharmaceutical companies, CROs, biotech firms

While both roles support clinical research, Clinical Study Coordinators focus on managing day-to-day site activities, whereas Clinical Research Associates primarily monitor and oversee multiple sites to ensure regulatory compliance and data integrity.

What cities near Oak Ridge, TN are hiring for Clinical Study Coordinator jobs?

Cities near Oak Ridge, TN with the most Clinical Study Coordinator job openings:

Clinical Study Coordinator jobs near you
Infographic showing various Clinical Study Coordinator job openings in Oak Ridge, TN as of August 2026, with employment types broken down into 3% As Needed, 68% Full Time, 20% Part Time, 8% Contract, and 1% Nights. Highlights an 93% Physical, 1% Hybrid, and 6% Remote job distribution, with an average salary of $64,573 per year, or $31 per hour.

Research Study Coordinator 1-Research Center (Knoxville)

The University of Tennessee

Knoxville, TN • On-site

$21.69/hr

Full-time

Re-posted 9 hours ago

Job description


Market Range: 08
Hiring Salary: $21.69/Hourly
THIS POSITION IS LOCATED IN KNOXVILLE, TN.
JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: The Research Study Coordinator 1 performs Investigator-Initiated Research for Maternal Fetal Medicine, Neonatology, and High-risk Obstetrics. This position assists the faculty with clinical research study activities including but not limited to the development, submission and management of regulatory paperwork, the submission of Institutional Review Board (IRB) applications and annual renewals, and preparation and maintenance of study files and essential trial documents
Responsibilities
  1. Assists investigators with the design of Maternal Fetal Medicine, Neonatology, and High-risk Obstetrics related studies by reviewing and/or writing proposals using methods best suited to study objectives.
  2. Assists investigators with the development and submission process for Institutional Review Board (IRB) approval including the collection of hospital collaboration agreements, key personnel documents, department approvals, funding source information, IRB application completion, and uploads in iMedRIS.
  3. Coordinates operational components of retrospective research and survey-driven research for study-specific Investigator-Initiated research for Maternal Fetal Medicine, Neonatology, and High-risk Obstetrics.
  4. Provides essential information to the GSM OB/GYN data coordinator, Physical Activity and Metabolism lab manager, or the Principal Investigator during the data analysis phase of Investigator-Initiated research.
  5. 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.
  6. 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.
  7. Establishes and maintains contact with study participants and families, community agencies, and health care providers.
  8. Assists investigator with the management and maintenance of study-specific Master Study Files and Essential Study Documents.
  9. Assists with the management and maintenance of Subject Source Documents.
  10. Facilitates study-specific communication and meetings.
  11. Performs other duties as assigned.

Qualifications
EDUCATION: Bachelor's Degree in 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.
  • Ability to interact with a diverse population.
  • Intermediate-level computer skills with the ability to learn new software applications for various electronic data capture programs.
  • Ability to exhibit strong interpersonal and communication skills.

Apply