Top 18 Clinical trial associate Jobs in Johnson City Tn

CRA 1, IQVIA Biotech
IQVIA —Elizabethton, TN
- $71,900 - $145,300 a year
- Full-time
- Bachelor's degree
- Travel
- Communication skills
Data Entry Coordinator - Lab Data Services
LabConnect, LLC —Johnson City, TN
- Online Application
- Office
- Travel
- Organizational skills
- AD&D insurance
- Paid holidays
Quick Apply
2d
Clinical Research Coordinator (8a-5p) Research Institute- Kingsport, TN
Ballad Health —Kingsport, TN
- Full-time
- Nursing
- Patient monitoring
- RN License
Project Coordinator
LabConnect, LLC —Johnson City, TN
- Online Application
- Hybrid work
- Word processing
- Computer literacy
- Basic math
- AD&D insurance
- Paid holidays
Quick Apply
8d
Clinical Trial Specialist
SOUTHEASTERN RETINA ASSOCIATES PC —Johnson City, TN
- 8 hour shift
- Surgery
- Mid-level
- In-person
- Health insurance
- Dental insurance
Quick Apply
Quality Audit Specialist
LabConnect, LLC —Johnson City, TN
- Online Application
- Remote
- Mid-level
- Bachelor's degree
- Continuous improvement
- AD&D insurance
- Paid holidays
Quick Apply
Research Assistant PT
Gastrointestinal Associates of Northeast Tennessee, PC —Johnson City, TN
- Part-time
- Blood sampling
- Computer skills
- LPN
Quick Apply
13d
Biospecimen Project Manager
LabConnect, LLC —Johnson City, TN
- Online Application
- Bachelor of Science
- Mid-level
- 3 years
- AD&D insurance
- Paid holidays
Quick Apply
Senior CRA
ICON Plc —Bristol, TN
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Travel
- Disability insurance
- Health insurance
Registered Nurse
Hawthorne Health, Inc. —Kingsport, TN
- Vital signs
- RN License
- English
Quick Apply
Senior Biospecimen Project Manager
LabConnect, LLC —Johnson City, TN
- Online Application
- Microsoft Word
- 5 years
- Computer literacy
- AD&D insurance
- Paid holidays
Quick Apply

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Data Entry Coordinator - Lab Data Services
LabConnect, LLC —Johnson City, TN
The Clinical Data and Laboratory Coordinator is responsible for ensuring the accuracy and timely reporting of clinical laboratory data, encompassing both the…
Quick Apply
2d
Project Coordinator
LabConnect, LLC —Johnson City, TN
Prolonged use of computer and headphones for conference calls. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with…
Quick Apply
8d

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CRA 1, IQVIA Biotech

IQVIA -
Elizabethton, TN

Apply Now

Job Details

Full-time
$71,900 - $145,300 a year

Qualifications

Regulatory compliance
Clinical audit and monitoring
ICH guidelines
Bachelor's degree
Clinical quality assurance standards
Oncology

Full Job Description

Elizabethton, United States of America | Full time | Field-based | R1534476

IQVIA Biotech is now hiring for CRA 1 with a minimum of 6 months of on-site monitoring. Must have experience monitoring in oncology solid tumor.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Job Overview

The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring high‑quality clinical data, and maintaining study integrity.

Key Responsibilities

As a CRA I, you will conduct various types of monitoring visits—including site selection, initiation, routine monitoring, and close‑out visits—to evaluate the quality and integrity of site practices. You will verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary. During these visits, you will review essential documents, assess protocol adherence, oversee data entry and query resolution, and ensure maintenance of both the Trial Master File (TMF) and the Investigator Site File (ISF).

A central part of this role involves building and maintaining strong communication with investigative sites. You will provide protocol training, set expectations, address site‑level challenges, and support recruitment planning to help sites meet enrollment targets. You will also collaborate closely with internal project teams to ensure cohesive study execution and may contribute to site-level financial processes or start‑up activities based on study needs.

Accurate and timely documentation is critical. The CRA I prepare detailed monitoring visit reports, follow‑up letters, and all required study documentation to ensure audit readiness and transparent oversight. The ability to manage multiple tasks, prioritize effectively, and work independently while maintaining productive team relationships is essential for success.

Qualifications

Bachelor’s degree required; a scientific or healthcare discipline is preferred.
6 months –2 years of relevant experience, with equivalent combinations of education, training, or completion of a CRA training program considered.
Basic knowledge of clinical research regulations (GCP/ICH).
Ability to travel as required by the project.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $71,900.00 - $145,300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Where you'll work

Field-based

You’ll work where the action is — out in the field, directly engaging with our customers, sites or partners. Field-based roles offer the opportunity to build relationships face-to-face, gain real-world insights and make a tangible impact.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Apply Now

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clinical trial associate jobs in johnson city tn

CRA 1, IQVIA Biotech

Data Entry Coordinator - Lab Data Services

Clinical Research Coordinator (8a-5p) Research Institute- Kingsport, TN

Project Coordinator

Clinical Trial Specialist

Quality Audit Specialist

Research Assistant PT

Biospecimen Project Manager

Senior CRA

Registered Nurse

Senior Biospecimen Project Manager

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