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Clinical Trials Associate Jobs in Tennessee (NOW HIRING)

Summary ROLE The Clinical Research Associate is an important member of the Alira Health Clinical ... clinical trials. CRAs work closely with the In-house CRAs, Lead CRAs, Director of Clinical ...

Clinic Administrative Assistant

Nashville, TN · On-site

$17.50 - $23.50/hr

Obtains, organizes, and maintains source documentation and medical records for clinical trials ... High School Diploma required, Associate Degree preferred * Basic Life Support Certificate preferred ...

Clinic Administrative Assistant

Nashville, TN

$17.50 - $23.50/hr

Obtains, organizes, and maintains source documentation and medical records for clinical trials ... High School Diploma required, Associate Degree preferred * Basic Life Support Certificate preferred ...

Clinic Administrative Assistant

Nashville, TN

$17.50 - $23.50/hr

Obtains, organizes, and maintains source documentation and medical records for clinical trials ... High School Diploma required, Associate Degree preferred * Basic Life Support Certificate preferred ...

... trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our ... BA/BS, in laboratory science, health science, or business; or an associate's degree with at least 2 ...

Ability to apply mathematical concepts to budget management for clinical trials. * Must have a working knowledge of Microsoft Office applications including word processing, Excel spreadsheets, and ...

$55 - $85/hr

Ability to apply mathematical concepts to budget management for clinical trials. * Must have a working knowledge of Microsoft Office applications including word processing, Excel spreadsheets, and ...

The Associate Clinic Research Nurse supports clinical research operations by delivering direct ... It has conducted more than 850 first-in-human clinical trials since its inception and contributed ...

The Associate Clinic Research Nurse supports clinical research operations by delivering direct ... It has conducted more than 850 first-in-human clinical trials since its inception and contributed ...

The Associate Clinic Research Nurse supports clinical research operations by delivering direct ... It has conducted more than 850 first-in-human clinical trials since its inception and contributed ...

The Associate Clinic Research Nurse supports clinical research operations by delivering direct ... It has conducted more than 850 first-in-human clinical trials since its inception and contributed ...

Serves as first point of contact for management issues related to clinical trials. * Works closely ... Associates degree (A.A/A.S) will be considered if combined with 3+ years of central laboratory ...

Showing results 21-40

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:

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.

Manager, Project Management

LabConnect

Johnson City, TN • On-site, Remote

Full-time

Medical, Life, Retirement, PTO

Posted 9 days ago


Job description

Overview
LabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world.
We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions.
Job Summary
The Manager of Project Management is responsible for assisting the department director with program implementation and evaluation of the Project Management division of LabConnect. This position may also manage and/or delegate responsibility for day-to-day oversight of ongoing clinical trial study projects. The Manager of Project Management assigns clinical trials study management responsibilities to a designated Project Manager, along with performing duties as project manager on their own assigned project manager projects. Working closely with Project Managers, the Manager of Project Management will direct activities to meet our client's specification and ensure quality deliverables on time and within budget. The Manager of Project Management may also serve in the capacity of a Project Manager to direct specific new clinical trial studies.
Essential Duties and Other Responsibilities
  • Serves as escalation point of contact for management issues related to clinical trials.
  • Writes, reviews and approves Project Management SOPs.
  • Works closely and in coordination with laboratory management and directors in support of clinical trials.
  • Direct supervision of Project Managers, Associate Project Managers, Project Coordinators and their respective clinical trials projects.
  • Assigns clinical trial protocols to Project Managers, following work requirements, to ensure quality and timely delivery of service.
  • Assists in hiring and assignment of Project Managers, Associate Project Managers and Project Coordinators.
  • Supervises, coaches, develops, and retains talented associates.
  • Analyzes and records personnel and operational data and writes related activity reports.
  • Meets with directors and other managers/supervisors to stay informed of changes affecting operations.
  • Ensures that all laboratory responsibilities outlined within the protocol are carried out in an efficient and professional manner and in compliance with laboratory policies.
  • Oversees creation of training materials for investigators and internal staff.
  • Oversees development of protocol and visit specific requisitions.
  • Interfaces with laboratory, customer service, business development, external project management, and information technology and data management personnel.
  • Represents LabConnect at bid defense meetings.
  • Provides departmental status updates to the department director.
  • Participates in internal quality assurance unit as a department head or SME as it pertains to client complaints, incidents, planned and unplanned deviations.
  • Performs Managerial duties approximately 50% of the time and Project Management duties approximately 50% of time for the first six months in the role; after six months in role performs Managerial duties approximately 80% of time and Project
  • Management duties approximately 20% of time. The percentage of time is subject to change based on business needs and leadership direction.
  • Performs other related duties and tasks as necessary or as assigned.

  • Education/Experience
  • Bachelor's degree from four-year college or university; and three years related clinical or laboratory experience and/or training; or equivalent combination of education and experience. Minimum three years central laboratory experience strongly preferred. Must be experienced in customer service and possess excellent organization and interpersonal, communication and problem-solving skills. Must be adept at stress management.

  • Certificates and Licenses:
  • Certification as an ASCP Medical Technologist or Medical Laboratory Technician is preferred. PMP certification preferred. Licensed Medical Laboratory Technologist/Technician (or equivalent) in the state of Tennessee preferred.

  • Required Skills
  • Excellent attention to details and ability to adapt to changing environments and requirements as well as customer service/client relationship management skills.
  • Ability to adhere to established timelines, processes and procedures.
  • Strong planning and problem-solving skills.
  • Self-motivating and ability to work well independently as well as using a collaborative team approach.
  • Excellent organization, time management skills, communication, multitasking, and interpersonal skills.
  • Excellent listening and verbal comprehension skills, including ability to translate client needs to team members.
  • Ability to make quick but well-thought out decisions.
  • Proficient in Microsoft Word, Excel, and database software.
  • Language Ability:
  • Ability to read, write and comprehend technically complex data transmission specification agreements, client correspondence, meeting agendas and meeting notes. This position requires that the incumbent be able to communicate with peers at client pharmaceutical and biotechnology firms in a professional manner that reflects well upon LabConnect, LLC.
  • Mathematical Ability:
  • Ability to apply simple mathematical skills and abstract thinking in a logical and organized manner.
  • Reasoning Ability:
  • Ability to solve practical problems, investigate client database issues using standard query tools and from the data generated draw correct and logical conclusions, use test scripts to validate newly authored project-specific data transmission routines; the ability to understand a variety of technical instructions, mathematical and diagrammatic representations of data in both an abstract and concrete manner.
  • Computer Skills:
  • To perform this job successfully, an individual must have working knowledge of Microsoft Office applications, including word processing software, spreadsheet software, database software and knowledge in the use of standard query tools is preferred.
  • Supervisory Responsibilities:
  • This job has supervisory responsibilities.
  • Work Environment:
  • The noise level in the work environment is usually moderate.
  • Physical Demands:
  • While performing the duties of this job, the employee is regularly required to sit. The employee is frequently required to talk or hear. The employee is occasionally required to stand; walk and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision and ability to adjust focus.

One Global Team
At LabConnect, we are proud to be one global team: united by our shared mission to advance clinical trials through innovation, agility, and collaboration. We believe that our people are our greatest asset, and we are committed to fostering a workplace that reflects our core values: People First, Quality Focused, Customer Centered, Technology Driven, and Accountability Always.
LabConnect is an Equal Opportunity Employer. We celebrate diversity and are dedicated to creating an inclusive environment for all employees. We do not discriminate based on race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), creed, national origin, age, disability, genetic information, veteran status, or any other legally protected status. We are committed to cultivating a workplace that is safe, equitable, and respectful for all. Together, as one global team, we strive to ensure that every individual has the opportunity to thrive and contribute to our shared success.
This job description should not be construed to imply that these requirements are the exclusive standards of the position. Incumbents will follow any other instructions and perform other related duties as may be required by their supervisor. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions of the job.
Join our team and discover how your work can impact patients' lives around the world!
Some of the Perks our LabConnectors Love:
  • Financial Security (Base Pay, 401k Match and Possible Annual Bonus Eligibility)
  • Health Benefits beginning on date of hire
  • PTO plan, plus 11 Paid Company Holidays, and 1 Day to Volunteer in your community
  • Short and Long-Term Disability, Life Insurance, and AD&D
  • We celebrate our differences, which enriches our culture!

In addition to great perks and challenging work assignments, we invest in our people with career growth opportunities, globally. We believe in a friendly and collaborative environment with open lines of communication. While living out our values of People First, Quality Focused, Customer Centered, Technology Driven, and Accountability Always.
We are proud to be an Equal Employment Opportunity Employer and value the diversity of our workforce. We do not discriminate on the basis of race, gender, age, disability, religion, sexual orientation, or any other protected characteristic. To learn more about equal employment opportunity, please view the posters here: https://www.dol.gov/agencies/whd/posters
LabConnect also prioritizes the privacy and security of your personal data. All candidate information is handled in accordance with General Data Protection Regulation (GDPR). To learn more, please review our Privacy Notice on our website, by navigating to https://www.labconnect.com/
If you need assistance to complete your job application, search for a job opening, or submit an online application at LabConnect, please email talent@labconnect.com or call +1 (423) 722-3155.