1

Study Management Associate Jobs in Tennessee (NOW HIRING)

... study specific questions * Review, enter, and edit patient information into clinical trial management software * Book patients into site schedulers ensuring that entries are accurate and up to date

... study specific questions * Review, enter, and edit patient information into clinical trial management software * Book patients into site schedulers ensuring that entries are accurate and up to date

Warehouse Associate II

Smyrna, TN

$15 - $17.75/hr

... management Individual Contributor Minimum Qualifications High School or GED General Studies or ... 000 associates. Based in Mooresville, N.C., Lowe's supports the communities it serves through ...

Warehouse Associate II

Smyrna, TN

$15 - $17.75/hr

... management * Individual Contributor Minimum Qualifications * High School or GED General Studies or ... 000 associates. Based in Mooresville, N.C., Lowe's supports the communities it serves through ...

next page

Showing results 1-20

Study Management Associate information

See Tennessee salary details

$10

$40

$58

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:
What cities in Tennessee are hiring for Study Management Associate jobs? Cities in Tennessee with the most Study Management Associate job openings:
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.
Quality Technician II, Welding - Jerome Ave

Quality Technician II, Welding - Jerome Ave

Astec Industries

Chattanooga, TN

$16.50 - $22/hr

Full-time

Posted 12 days ago


Astec rating

7.5

Company rating: 7.5 out of 10

Based on 44 frontline employees who took The Breakroom Quiz

216th of 415 rated machine equipment manufacturers


Job description

Description
BUILT TO CONNECT
Astec is a global, environmentally focused infrastructure and manufacturing company of asphalt road building and aggregate processing. Our mission is to design and build the most innovative products for the industries we serve. Leveraging innovative solutions and technologies, we serve customers all over the world.
ABOUT THE POSITION
The Quality Technician is an operational position responsible for executing and delivering best in class quality functions including but not limited to the inspection of in-coming raw materials, in-process materials, documenting the batching, mixing, and manufacturing process, ensuring product consistency and quality and the inspection of final product prior to shipment to the customer. This position works closely with other departments to resolve quality issues.
Key Deliverables
Conduct Inspection checks on products and production processes.
Perform manual and automated quality checks.
Maintain accurate report of any issues that may arise.
Identify issues and the steps needed to resolve the issue.
Adhere to Astec quality standards.
Key Activities & Responsibilities
Serve as a quality technical advisor for each Manufacturing Bay and Field Service personnel.
Engage with product teams directly to review systemic quality issues, assist with root cause analysis and corrective action implementation
Review Work Orders and subsequent Supplements to ensure equipment is manufactured as specified.
Execute inspection criteria to verify industry and Astec quality standards.
Perform Receiving, In-Process, Final and Functional inspections.
Collaborate with Fitter/Welders to identify drawing / process changes affecting product quality.
Identify actions needed for improvement on the provided task lists.
Update the Quality chart on the assigned task list daily.
Support Product / Manufacturing / Quality Engineers as a "First Responder" to address issues identified.
Prepares quality documentation and reports by collecting, analyzing, and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations.
Maintain cleanliness in designated workspace by practicing 6S principles to reduce safety risks.
Maintain a safe work environment and ensure that all company safety procedures are followed to include OSHA compliance guidelines applicable to the duties above.
Attend a weekly department safety meeting.
Understand the histogram data to help the team identify primary issues affecting the team's performance to goals.
Update controlled documents.
Maintain and improve quality performance metrics and/or quality records including first pass yield.
Track all significant product, document, and process changes which affect quality.
Perform employee, work center, and piece audits as required.
Perform process audits to insure conformity of parts to specifications.
To be successful in this role, your experience and competencies are:
High school diploma or general education degree (GED) or a combination of education and experience equivalent as deemed sufficient by management.
Associate of Art's degree (A.A.) from two-year College or similar degree from a technical school, desirable but not required.
Certified Quality Technician (ASQ) or other professional certifications desired.
4-6 years' experience as a Quality Technician in a heavy manufacturing industry; mechanical background in hydraulics, diesel engines, or electronics; or demonstrated abilities through experience or education.
1-3 years' experience working with ISO or similar quality/inspection experience.
Maintain positive, cooperative working relationships by working, acting, and communicating with various personalities getting along with customers, vendors, co-workers, and management working both individually and as part of a team.
Consistently administers established policies and procedures. Must exercise tact and professionalism when interacting with employees in this regard.
Skill in working efficiently and accurately to keep up with production requirements.
Capacity to learn quickly, flexible, and adaptable in coping with pressures, deadlines, and rapidly changing situations in a fast-paced work environment.
Experience in writing, documenting processes and procedures, and attention to detail preferred.
Able to execute job tasks based on verbal instructions, written procedures or by following engineering specifications from drawings.
Strong written and verbal communication skills and the ability to interact across all levels of the organization.
Capable of exercising solid judgment and decision-making during inspection process and taking appropriate action to resolve any quality issues or concerns during the inspection process or otherwise.
Supervisor and Leadership Expectations
None
Our Culture and Values
Employees that become part of Astec embody the values below throughout their work.
Continuous devotion to meeting the needs of our customers
Honesty and integrity in all aspects of business
Respect for all individuals
Preserving entrepreneurial spirit and innovation
Safety, quality and productivity as means to ensure success
Travel Requirements: % of travel, regional, international
WORK ENVIRONMENT
Manufacturing Environment
Shop manufacturing environment exposures include exposure to moving mechanical parts, machinery, tools and equipment, vibration, fumes or airborne particles, motorized vehicles, welding and machining operations, outside weather conditions and exposure to the risk of electric shock. The employee may occasionally be exposed to varying levels of dirt, dust, toxic or caustic chemicals, very warm and/or very chilly temperatures. The noise level in the shop can be very loud at times consistent with an industrial assembly facility and may require hearing protection. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
EQUAL OPPORTUNITY EMPLOYER

What Astec employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom