ZipRecruiter

Log In

1

Clinical Trials Associate Jobs in Tennessee (NOW HIRING)

DelRicht Research

Medical Assistant

Nashville, TN

$55K/yr

Our clinical trials provide new treatment options for our patients and ultimately our goal is to ... Bachelor's or Associate's degree from an accredited college or university. * This is an onsite ...

DelRicht Research

Medical Assistant

Hendersonville, TN · On-site

$55K/yr

Our clinical trials provide new treatment options for our patients and ultimately our goal is to ... Bachelor's or Associate's degree from an accredited college or university. * This is an onsite ...

labconnect

Clinical Sample Specialist

Johnson City, TN · On-site

BA/BS, in laboratory science, health science, or business; or an associate's degree with at least 2 ... to advance clinical trials through innovation, agility, and collaboration. We believe that our ...

LabConnect

Customer Care Specialist

Johnson City, TN · On-site

$16.25 - $21.50/hr

... clinical trials and laboratory operations. * Other duties as assigned. Education and Experience * High school diploma or equivalent required; associate or bachelor's degree preferred. * Previous ...

LabConnect

Manager, Proposals

Johnson City, TN · On-site +1

Ability to apply mathematical concepts to budget management for clinical trials. * Ability to manage a team of Proposal Managers and Associates. * Ability to read, analyze, and interpret general ...

LabConnect

Manager, Proposals

Johnson City, TN · On-site

$85 - $120/hr

Ability to apply mathematical concepts to budget management for clinical trials. * Ability to manage a team of Proposal Managers and Associates. * Ability to read, analyze, and interpret general ...

previous page

Showing results 41-60

All JobsClinical Trials Associate JobsClinical Trials Associate Jobs in Tennessee

Clinical Trials Associate information

See Tennessee salary details

$15

$36

$63

How much do clinical trials associate jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical trials associate in Tennessee is $36.29, according to ZipRecruiter salary data. Most workers in this role earn between $29.23 and $39.90 per hour, depending on experience, location, and employer.

What is a clinical trials associate?

Clinical Trials Associates (CTAs) are professionals who support the planning, coordination, and administration of clinical research studies, often working under the supervision of Clinical Research Coordinators or Managers. Their responsibilities typically include maintaining study documentation, ensuring regulatory compliance, assisting with data collection, and communicating with study sites. CTAs play a critical role in ensuring that clinical trials run smoothly and adhere to strict protocols and guidelines. Their work helps bring new medical treatments and therapies to market safely and efficiently.

What are the key skills and qualifications needed to thrive as a clinical trials associate, and why are they important?

To thrive as a Clinical Trials Associate, you need a solid understanding of clinical research protocols, regulatory compliance, and data management, typically supported by a life sciences degree. Familiarity with systems such as electronic data capture (EDC), clinical trial management systems (CTMS), and knowledge of Good Clinical Practice (GCP) guidelines or related certifications is important. Strong organizational skills, attention to detail, and effective communication help you excel in coordinating study activities and collaborating with diverse teams. These skills ensure accurate trial execution, regulatory adherence, and successful study outcomes.

What are some common challenges faced by clinical trials associates, and how can they be managed effectively?

Clinical Trials Associates often face challenges such as coordinating with multiple stakeholders, managing tight deadlines, and ensuring strict compliance with regulatory guidelines. Balancing administrative tasks with participant communication requires strong organizational skills and attention to detail. Staying proactive in communication, utilizing project management tools, and seeking guidance from senior team members can help manage these challenges effectively while fostering a collaborative team environment.

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

AspectClinical Trials AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like ACRP or SOCRA are commonBachelor's degree in health sciences or related field; certifications like CCRP are advantageous
Work EnvironmentTypically works in clinical trial sites, pharmaceutical companies, or CROsWorks directly at clinical sites, hospitals, or research centers
Job FocusSupports trial setup, data entry, and regulatory complianceManages patient recruitment, scheduling, and data collection

While both roles support clinical research, Clinical Trials Associates primarily focus on trial logistics and compliance, whereas Clinical Research Coordinators handle patient interactions and site management. Both positions require similar educational backgrounds and certifications, often working in the same environments, but their daily responsibilities differ.

Is a clinical trials associate a good career?

A clinical trials associate is a valuable role in the healthcare and pharmaceutical industries, responsible for coordinating and monitoring clinical trial activities. It offers opportunities for career growth, requires attention to detail, and often involves working with regulatory guidelines and data management tools. The role can be stable and rewarding for those interested in medical research and patient safety.

What do I need to be a clinical trials associate?

To become a clinical trials associate, candidates typically need a bachelor's degree in life sciences, healthcare, or a related field. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with clinical trial management systems or regulatory documentation. Certifications such as the Certified Clinical Research Professional (CCRP) can enhance job prospects.

What are the most commonly searched types of Clinical Trials jobs in Tennessee?

The most popular types of Clinical Trials jobs in Tennessee are:

What cities in Tennessee are hiring for Clinical Trials Associate jobs?

Cities in Tennessee with the most Clinical Trials Associate job openings:

Clinical Trials Associate jobs near you
Infographic showing various Clinical Trials Associate job openings in Tennessee as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 23% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $75,486 per year, or $36.3 per hour.

Physician Pediatric-Endocrinology - Competitive Salary

Vanderbilt University Medical Center

Nashville, TN • On-site

Other

Re-posted 8 days ago

Key responsibilities

  • Provide inpatient consultative care and outpatient management for the full spectrum of pediatric endocrine disorders

  • Share coverage in both the Pediatric Endocrinology and Pediatric Diabetes clinics on the main campus

  • Teach and mentor medical students, residents, and fellows in ACGME‑accredited training programs

Vanderbilt University Medical Center rating

7.4

Company rating: 7.4 out of 10

Based on 258 frontline employees who took The Breakroom Quiz

267th of 898 rated healthcare providers

Job description

The Vanderbilt University Medical Center (VUMC) Department of Pediatrics seeks a faculty member in the Ian M. Burr Division of Pediatric Endocrinology & Diabetes at the Assistant or Associate Professor level on the Clinical Educator (CE) or Clinical Practice (CP) tracks. Responsibilities include direct patient care in both inpatient and ambulatory settings, teaching of students, residents, and fellows, and participation in clinical research and/or quality improvement initiatives.


Among the largest pediatric endocrinology programs in the Southeast, the Division conducts over 22,000 outpatient visits annually. All physicians provide care in both our Pediatric Endocrinology and Pediatric Diabetes clinics on main campus and participate in a strong outreach network across seven offsite locations in Middle Tennessee.


Key Responsibilities

  • Provide inpatient consultative care and outpatient management for the full spectrum of pediatric endocrine disorders
  • Share coverage in both the Pediatric Endocrinology and Pediatric Diabetes clinics on the main campus
  • Participate in regional outreach clinics (Middle Tennessee), within driving distance from Nashville
  • Teach and mentor medical students, residents, and fellows in ACGME‑accredited training programs
  • Engage in clinical research and/or quality improvement; collaborate with multidisciplinary teams and research staff
  • Contribute to program development across subspecialty clinics (e.g., Turner Syndrome, Metabolic Bone Disease, Lipid Disorders, DSD, Prader‑Willi, Pediatric Head & Neck Endocrine Cancer, ALD, DMD)—program portfolio captured in your intake form
  • Predominantly outpatient; inpatient service/consults rotate periodically
  • Advanced Practice Support: NPs practice independently; no routine mid‑level supervision required  

Qualifications

  • MD/DO (or equivalent) and Tennessee medical licensure (or eligibility)
  • Board certified or board eligible in Pediatric Endocrinology
  • Demonstrated excellence in clinical care, education, and scholarship
  • Leadership/organizational strength and commitment to collaboration, mentorship, and clinical excellence
  • Dual training in Med‑Peds Endocrinology welcomed

About the Ian M. Burr Division of Pediatric Endocrinology & Diabetes

  • Among the largest pediatric endocrinology clinical and research programs in the Southeast, delivering 22,000+ outpatient visits annually
  • Children’s Diabetes Program follows 4,000+ patients, spanning Prediabetes, CF‑Related Diabetes, Type 1 and Type 2 programs, and a Type 1 Diabetes Immunotherapy Clinic
  • ADA‑recognized Diabetes Self‑Management Education program, staffed by Certified Diabetes Care & Education Specialists (CDCES), pump specialists, and registered dietitians
  • Robust clinical trials infrastructure with 49 active studies (27 diabetes; 22 metabolic bone disease/obesity) and membership as a Type 1 Diabetes TrialNet Clinical Center—the intake confirms the scale of active trials and research footprint

About Vanderbilt University Medical Center & Monroe Carell Jr. Children’s Hospital

  • The Department of Pediatrics includes ~500 faculty/providers and is consistently in the Top‑10 for NIH funding among U.S. medical schools, offering a rich environment for multidisciplinary care, education, and research
  • Monroe Carell Jr. Children’s Hospital at Vanderbilt is ranked in 10 of 11 pediatric specialties in U.S. News & World Report 2024–2025 and is expanding from 325 to 400+ beds as two additional floors near completion
  • The Division supports an ACGME‑approved fellowship and integrates with VUMC’s extensive research cores, biostatistics, and clinical trials infrastructure; your intake notes the fellowship accreditation and trial activity within the Division

How to Apply

Please submit your CV and a brief letter of interest. Applications will be reviewed on a rolling basis. Start date is negotiable. Please apply directly or send CV and LOI to Physician Recruiter, Sarah Casen.

 

Vanderbilt Health is committed to fostering an environment where everyone has the chance to thrive and is committed to the principles of equal opportunity.  EOE/Vets/Disabled.

What Vanderbilt University Medical Center employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply