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Clinical Trial Assistant Jobs in Decatur, GA (NOW HIRING)

Denali Health

Clinical Research Coordinator III

Atlanta, GA · On-site

$23.25 - $31/hr

Experience with EDC systems and clinical trial management software preferred. * CCRC/CCRP ... certification a plus. Why Join Denali Health: * Work with a mission-driven team advancing clinical ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

This position offers flexible scheduling while providing critical support to our clinical trial ... Coordinate with Principal Investigators, study coordinators, sponsors, and CROs * Assist with ...

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

This position offers flexible scheduling while providing critical support to our clinical trial ... Coordinate with Principal Investigators, study coordinators, sponsors, and CROs * Assist with ...

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All JobsClinical Trial JobsClinical Trial Assistant JobsClinical Trial Assistant Jobs in Decatur, GA

Clinical Trial Assistant information

See Decatur, GA salary details

$11

$36

$67

How much do clinical trial assistant jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical trial assistant in Decatur, GA is $36.78, according to ZipRecruiter salary data. Most workers in this role earn between $25.10 and $46.92 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical trial assistant?

To thrive as a Clinical Trial Assistant, you need a solid understanding of clinical research processes, attention to detail, and a relevant degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, trial management software, and knowledge of Good Clinical Practice (GCP) guidelines are typically required. Strong organizational skills, effective communication, and the ability to multitask help you excel in supporting clinical trial operations. These skills ensure protocol compliance, data accuracy, and smooth coordination within clinical research teams.

What does a clinical trial assistant do?

A clinical trial assistant is responsible for monitoring the medical and administrative procedures during a clinical trial. In this career, you prepare patients for tests, take blood, perform laboratory work, prep for medical treatments, and collect data for research. You work with project managers and research associates throughout the beginning, implementation, and closeout of the trial. You also handle paperwork, file records, prepare reports, label medication, track progress, and fulfill other duties that arise during medical studies. You may assist with appointment schedules, plan meetings, and communicate with external sources and investigators as well.

What is the difference between Clinical Trial Assistant vs Clinical Research Coordinator?

AspectClinical Trial AssistantClinical Research Coordinator
ResponsibilitiesSupports trial logistics, manages documentation, assists with regulatory complianceOversees study conduct, recruits participants, manages site operations
CredentialsTypically requires a bachelor's degree in health or life sciencesOften requires a bachelor's or master's degree in health sciences or related fields
Work EnvironmentResearch sites, sponsor offices, clinical trial centersClinical sites, hospitals, research institutions
Industry UsageCommonly employed in pharmaceutical companies, CROs, research institutionsPrimarily in hospitals, clinics, research centers

The Clinical Trial Assistant primarily supports trial logistics and documentation, working closely with the research team. In contrast, the Clinical Research Coordinator manages the overall conduct of the study, including participant recruitment and site management. Both roles require similar educational backgrounds but differ in scope and responsibilities within the clinical research process.

What is a clinical trial assistant?

Clinical Trial Assistants (CTAs) are professionals who provide administrative support to clinical research teams during the planning, execution, and close-out of clinical trials. They help ensure that studies comply with regulatory standards, maintain accurate documentation, and coordinate communication between different stakeholders. CTAs often manage trial master files, track study progress, and assist with scheduling meetings and site visits. Their work is essential to the smooth operation of clinical studies and the integrity of collected data.

What are some typical challenges a clinical trial assistant may face when supporting multiple trials simultaneously?

Clinical Trial Assistants often support several studies at once, which can make time management and organization challenging. Balancing competing priorities, meeting tight regulatory deadlines, and ensuring accurate documentation are common hurdles. Effective communication with study coordinators, principal investigators, and sponsors is essential to keep all parties informed and processes running smoothly. Proactively using organizational tools and regularly updating tracking systems can help manage this fast-paced environment.
More about Clinical Trial Assistant jobs
What are the most commonly searched types of Clinical Trial jobs in Decatur, GA? The most popular types of Clinical Trial jobs in Decatur, GA are:
What are popular job titles related to Clinical Trial Assistant jobs in Decatur, GA? For Clinical Trial Assistant jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Assistant jobs in Decatur, GA look for? The top searched job categories for Clinical Trial Assistant jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Trial Assistant jobs? Cities near Decatur, GA with the most Clinical Trial Assistant job openings:
Clinical Trial Assistant jobs near you
Infographic showing various Clinical Trial Assistant job openings in Decatur, GA as of August 2026, with employment types broken down into 2% As Needed, 74% Full Time, 16% Part Time, 2% Temporary, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $76,493 per year, or $36.8 per hour.

Clinical Research Coordinator I/II/III Opportunities - Multiple Locations Nationwide

Headlands Research

Atlanta, GA • On-site

$45K - $100K/yr

Full-time

Re-posted 11 days ago

Job description

At Headlands Research, we are dedicated to enhancing clinical trial delivery within our communities. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation. Founded in 2018, our rapidly growing company currently operates 20+ sites across the US and Canada, with plans for further expansion.
About the Opportunity
We're always interested in connecting with individuals who are curious about, experienced in, or eager to begin a career in clinical research.
This general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide.
Clinical Research Coordinators are at the heart of our work. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.
Our Process
When you apply to this posting, your profile is reviewed by our Talent Acquisition team and kept on file for current and upcoming CRC opportunities. As new roles open, we proactively match candidates based on location preference, education, experience, and career interests. If there's a strong fit, a member of our team will reach out to start the conversation.
What CRC Roles Look Like at Our Company
Clinical Research Coordinators support the day-to-day execution of clinical trials. This includes working directly with patients, coordinating study visits, collecting and managing data, and ensuring studies are conducted in compliance with protocols and regulatory requirements. CRCs work closely with investigators, patients, and cross-functional teams, gaining exposure to a wide range of therapeutic areas and research processes. Roles may vary based on experience level and site needs, with opportunities to grow and take on increasing responsibility over time.
Who We're Looking For
We welcome interest from candidates who bring:
  • A bachelor's degree in a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or
  • Hands-on experience in lab courses, research projects, or clinical settings (internships, volunteering, or academic labs)
  • Strong attention to detail and the ability to follow structured protocols
  • Excellent organizational and time management skills
  • Clear communication skills and comfort interacting with patients and team members
  • A genuine interest in healthcare, research, or improving patient outcomes
  • Prior experience as a CRC is required for some locations

Why Start or Grow Your Career in Clinical Research with Us
  • A strong entry point into the clinical research and healthcare industry
  • Hands-on experience working with patients and clinical trial protocols
  • Opportunities to learn GCP, regulatory processes, and study operations
  • Mentorship and training to help you build a long-term career in research
  • Clear pathways for growth into CRCII, III, and senior, regulatory, or leadership roles
  • The chance to contribute to the development of new treatments that impact patients' lives
Ready to Start the Conversation?
Whether you're an experienced coordinator or a recent graduate looking to apply your lab and academic experience in a real-world setting, we'd love to hear from you.
Apply here to be considered for current and future Clinical Research Coordinator opportunities. Our Talent Acquisition team will reach out as roles become available that align with your background and interests.
California Pay Range
$45,000-$100,000 USD
Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver's license information, etc) via email or messenger tools, or for a financial deposit of any kind.
Headlands Research is an Equal Opportunity Employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability status, genetic information, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.
Need Assistance?
Headlands Research is committed to providing access and reasonable accommodation in its employment for individuals with disabilities. To request disability accommodation in the application process, contact recruiting@headlandsresearch.com for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

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