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Study Management Associate Jobs in Tennessee (NOW HIRING)

The Georgetown University

$44.02K - $73.41K/yr

Requirements Job Overview The Manager of Financial Aid Loans and Work-Study, under the general oversight of the Senior Associate Director, provides financial aid awarding and counseling services to ...

Eisai, Inc

$224.60K - $294.74K/yr

... studies across the product portfolio. Works closely with his/her direct reports in the field ... Assists other managers (Associate Directors) with leadership competency criteria including ...

New

McKesson

Director Study Operations

Nashville, TN

You will manage and direct the efforts of managers and recommend colleague actions including, but ... An Associate's degree, Bachelor's degree preferred * At least one year of leadership experience in ...

McKesson

Director Study Operations

Nashville, TN

You will manage and direct the efforts of managers and recommend colleague actions including, but ... An Associate's degree, Bachelor's degree preferred * At least one year of leadership experience in ...

Mckesson

Director Study Operations

Nashville, TN

You will manage and direct the efforts of managers and recommend colleague actions including, but ... An Associate's degree, Bachelor's degree preferred * At least one year of leadership experience in ...

Thompson Thrift

Traveling Superintendent

Gallatin, TN

Bachelor's or Associate's degree in construction management, civil engineering, or related field of study. An equivalent level of education and experience will be considered. * Experience: * Bachelor ...

New

Southeastern Freight Lines

Management Trainee

Memphis, TN

$50K - $60K/yr

As a Management Trainee, you will participate in our Operations Management Trainee Program. This is ... study. Interface with appropriate Support Center and Service Center associates in the completion of ...

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How much do study management associate jobs pay per hour?

As of May 30, 2026, the average hourly pay for study management associate in Tennessee is $40.74, according to ZipRecruiter salary data. Most workers in this role earn between $26.93 and $53.14 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Study Management Associate, and why are they important?

To thrive as a Study Management Associate, you need strong organizational skills, attention to detail, and a background in life sciences or clinical research, often supported by a relevant bachelor's degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines such as GCP are typically required. Effective communication, time management, and problem-solving abilities help facilitate collaboration among cross-functional teams and ensure smooth study execution. These skills are crucial for maintaining the quality, compliance, and efficiency of clinical studies.

What are the typical responsibilities of a Study Management Associate in a clinical research team?

As a Study Management Associate, you will play a key role in supporting clinical trials by coordinating study logistics, maintaining essential documentation, and ensuring compliance with regulatory guidelines. Your daily tasks may include organizing meetings, tracking study progress, preparing reports, and liaising with clinical sites and vendors. You will work closely with study managers, clinical research associates, and data management teams to ensure trials run smoothly and efficiently. This collaborative environment provides valuable exposure to various aspects of clinical research and can serve as a strong foundation for career advancement within the industry.

What is a Study Management Associate?

A Study Management Associate is a professional who supports the planning, coordination, and execution of clinical trials or research studies. They typically assist study managers or project leads by handling administrative tasks, maintaining study documentation, and ensuring compliance with regulatory guidelines. Their responsibilities may include scheduling meetings, tracking study progress, managing study supplies, and liaising with study sites or vendors. This role is essential for keeping research studies organized and running efficiently.

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

AspectStudy Management AssociateClinical Research Coordinator
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, often with certifications like CCRP
Work EnvironmentPharmaceutical companies, CROs, research institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed in industry-sponsored trials and clinical research firmsCommon in academic and hospital-based studies
Search & Comparison IntentHigh overlap in job duties and qualificationsSimilar roles with some operational differences

The Study Management Associate and Clinical Research Coordinator roles share many similarities, including required education and work environments. However, the Study Management Associate typically focuses on supporting study operations within industry settings, while the Clinical Research Coordinator often manages patient interactions and site activities in clinical settings. Both roles are essential in advancing clinical research but differ slightly in scope and daily responsibilities.

What are popular job titles related to Study Management Associate jobs in Tennessee? For Study Management Associate jobs in Tennessee, the most frequently searched job titles are:
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What cities in Tennessee are hiring for Study Management Associate jobs? Cities in Tennessee with the most Study Management Associate job openings:
Study Management Associate jobs near you
Infographic showing various Study Management Associate job openings in Tennessee as of May 2026, with employment types broken down into 91% Full Time, 6% Part Time, 1% Contract, and 2% Nights. Highlights an 93% Physical, 5% Hybrid, and 2% Remote job distribution, with an average salary of $84,736 per year, or $40.7 per hour.
Research Study Coordinator-Research Center (Knoxville)

Research Study Coordinator-Research Center (Knoxville)

The University of Tennessee

Knoxville, TN

$21.69/hr

Full-time

Posted 19 days ago

Job description

Market Range: 08

Hiring Range: $21.69/Hourly

THIS IS A TWO YEAR GRANT-FUNDED POSITION LOCATED IN KNOXVILLE, TN.

JOB SUMMARY/ESSENTIAL JOB FUNCTIONS:  Under the direction of the GSM Director of Research, the Research Study Coordinator 1 performs as the Research Study Coordinator for Investigator-Initiated Research. 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.

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 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.
  1. Assists investigators with the development of design studies by reviewing proposals to determine best-suited methods for study objectives.
  2. Assist investigators with the collection and submission process for initial Institutional Review Board (IRB) submissions including the collection of hospital collaboration agreements, key personnel documents, department approvals, funding source information, Investigational New Drug (IND) information, Drug(s)/Device(s) specifics, and IRB application completion and upload into iMedRIS.
  3. Assists investigator with the IRB Continuing Review process that includes the completion of study status reports.
  4. Prepares study-specific protocols, source documents/spreadsheets, drafts of required study logs and essential trial documents, and prepares files.
  5. Assists investigator with the execution and coordination of GSM Investigator-Initiated Research.
  6. Assists in screening potential subjects, reviewing and documenting patient medical histories and concurrent medication lists, obtaining informed consent from patients, 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 Trial File and Essential Trial Documents. 
  9. Assists investigators and the Director of Research with the coordination of Quality Assurance and Monitoring pathway audits.
  10. Performs other duties assigned. 

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