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Temporary Clinical Trials Test Subject Jobs in Decatur, GA

Care Access

Clinical Research Coordinator II

Decatur, GA · On-site

$23.75 - $31.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Strong computer skills with demonstrated abilities using clinical trials database, IVR systems ... TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT ...

Care Access

Clinical Research Coordinator II

Decatur, GA · On-site

$23.75 - $31.50/hr

Strong computer skills with demonstrated abilities using clinical trials database, IVR systems ... TEST. AN EMPLOYER WHO VIOLATES THIS LAW IS GUILTY OF A MISDEMEANOR AND SUBJECT TO A FINE NOT ...

CenExel

Principal Investigator - Internal Medicine

Decatur, GA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of ... Evaluate subject safety and compliance with the investigational product as specified in the ...

Thermo Fisher Scientific

Psychometrist

Atlanta, GA · On-site

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Ensure subject safety by appropriately responding to any potential for harm to self or others ...

Thermo Fisher Scientific

Psychometrist

Atlanta, GA

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for ... Ensure subject safety by appropriately responding to any potential for harm to self or others ...

Syneos Health

CRC II (Onsite) - Marietta, GA

Marietta, GA · On-site

$23 - $30.50/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Manage multiple clinical trials simultaneously. * Protect the safety of human subjects. * Monitor ... subject or study issues and escalate as appropriate. * Prepare for and participates in sponsor ...

Georgia Tech

Oncology Clinical Research Nurse

Atlanta, GA · On-site

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Evaluation & Implementation of Clinical Trials Review study protocols, primary disease category ... Conduct of Study Schedule patient visits, laboratory tests and procedures; Under the direction of ...

Emory Healthcare

NP/PA, Survivorship Clinic

Decatur, GA · On-site

$106K - $137K/yr

  • Medical

Comprehensive health benefits that start Day 1 Winship Clinical Trials Team Our Winship Clinical ... Orders, schedules and/or performs laboratory tests and diagnostic procedures. MINIMUM ...

Alcanza Clinical Research

Part-time Pharm Tech

Decatur, GA · On-site

$17 - $20.75/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Integration of investigational medication use, pharmacy workflow, subject medication safety ... Because all approved medications require clinical trials, the impact of your work is exponential ...

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Showing results 21-40

All JobsClinical Trials Test Subject JobsTemporary Clinical Trials Test Subject JobsTemporary Clinical Trials Test Subject Jobs in Decatur, GA

Temporary Clinical Trials Test Subject information

See Decatur, GA salary details

$15

$52

$87

How much do temporary clinical trials test subject jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for temporary clinical trials test subject in Decatur, GA is $52.90, according to ZipRecruiter salary data. Most workers in this role earn between $33.56 and $79.57 per hour, depending on experience, location, and employer.

What is the difference between Temporary Clinical Trials Test Subject vs Clinical Research Coordinator?

AspectTemporary Clinical Trials Test SubjectClinical Research Coordinator
CredentialsNo formal certifications typically required; must meet trial-specific criteriaUsually requires a bachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentParticipates in clinical trials, often in medical facilities or research centersWorks in research sites, hospitals, or clinics managing trial operations
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, pharmaceutical companies
Search & Comparison IntentUnderstanding trial participation rolesManaging and coordinating clinical trials

The main difference is that Temporary Clinical Trials Test Subjects participate in trials without requiring extensive certifications, focusing on trial participation. Clinical Research Coordinators, however, manage and oversee the trial process, often needing relevant certifications and experience. Both roles are essential in clinical research but serve different functions within the industry.

What are popular job titles related to Temporary Clinical Trials Test Subject jobs in Decatur, GA? For Temporary Clinical Trials Test Subject jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Temporary Clinical Trials Test Subject jobs in Decatur, GA look for? The top searched job categories for Temporary Clinical Trials Test Subject jobs in Decatur, GA are:
Temporary Clinical Trials Test Subject jobs near you
Infographic showing various Temporary Clinical Trials Test Subject job openings in Decatur, GA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $110,027 per year, or $52.9 per hour.

Clinical Research Coordinator I (ETS)| Temporary

Emory Healthcare

Atlanta, GA • On-site

$23.50 - $31.50/hr

Part-time

Re-posted 12 days ago

Emory Healthcare rating

7.7

Company rating: 7.7 out of 10

Based on 217 frontline employees who took The Breakroom Quiz

157th of 887 rated healthcare providers

Job description

Overview
Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future. We welcome candidates who can contribute to the excellence of our academic community.
Description
The Clinical Research Coordinator handles or assists with the administrative activities generally associated with the conduct of clinical trials.
KEY RESPONSIBILITIES:
  • Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
  • Assists with patient recruitment.
  • Attends study meetings.
  • Orders and maintains equipment and supplies.
  • Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
  • Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
  • Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
  • Assists with quality assurance and tracks regulatory submissions.
  • Performs related approved responsibilities as required.

ADDITIONAL JOB DUTIES:
  • Handles or assists with administrative activities generally associated with the conduct of clinical trials.
  • Maintains data pertaining to research projects, completes source documents/case report forms, and performs data entry.
  • Assists with patient recruitment.
  • Attends study meetings.
  • Orders and maintains equipment and supplies.
  • Reviews medical records and/or conducts screenings for recruitment of study participants, performs interviews and QOL questionnaires.
  • Collects study specimen according to protocol which may include phlebotomy, processing, and preparation for shipping.
  • Coordinates services, schedules procedures, creates and maintains case packages, and monitors charges.
  • Assists with quality assurance and tracks regulatory submissions.
  • Performs related approved responsibilities as required.

MINIMUM QUALIFICATIONS:
  • High School Diploma or GED and three years of administrative support experience.
  • Or two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience.
  • Or be a licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience.
  • Or a Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program.

This position is intended to support clinical research and all clinical training requirements must be tracked and monitored through Emory Healthcare under the credentialing category of Clinical Researcher.
NOTE: Position tasks are required to be performed in-person at an Emory University location; working remote is not an option. Emory reserves the right to change this status with notice to employee.
Additional Details
Emory is an equal opportunity employer, and qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law. Emory University does not discriminate in admissions, educational programs, or employment, including recruitment, hiring, promotions, transfers, discipline, terminations, wage and salary administration, benefits, and training. Students, faculty, and staff are assured of participation in university programs and in the use of facilities without such discrimination. Emory University complies with Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veteran's Readjustment Assistance Act, and applicable executive orders, federal and state regulations regarding nondiscrimination, equal opportunity, and affirmative action (for protected veterans and individuals with disabilities). Inquiries regarding this policy should be directed to the Emory University Department of Equity and Civil Rights Compliance, 201 Dowman Drive, Administration Building, Atlanta, GA 30322. Telephone: 404-727-9867 (V) | 404-712-2049 (TDD).
Emory University is committed to ensuring equal access and providing reasonable accommodations to qualified individuals with disabilities upon request. To request this document in an alternate format or to seek a reasonable accommodation, please contact the Department of Accessibility Services at accessibility@emory.edu or call 404-727-9877 (Voice) | 404-712-2049 (TDD). We kindly ask that requests be made at least seven business days in advance to allow adequate time for coordination.

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