ZipRecruiter

Log In

1

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

Denali Health

Clinical Research Nurse

Atlanta, GA · On-site

We conduct Phase I-IV clinical trials across multiple therapeutic areas, including neurology ... Coordinate with Principal Investigators, study coordinators, sponsors, and CROs * Assist with ...

Georgia Institute of Technology

Research Assistant

Atlanta, GA · On-site

$18.50 - $25.50/hr

Clinical Trials Research Assist faculty members (PIs, CO-ls, etc.) and the Research Manager in conducting new, extramurally funded clinical trials and assists in coordinating clinical trial research ...

OneOncology LLC

Clinical Medical Assistant

Johns Creek, GA · On-site

$16.75 - $21.25/hr

... of clinical trials. Applies knowledge gained to execute tasks prescribed by the trial ... Clinical Medical Assistant will have access to PHI and ePHI in the course of his/her duties.

Emory University

Pediatric BMT Clinician

Atlanta, GA · On-site

$165K - $214K/yr

Rank of assistant or associate professor will depend on experience and accomplishments. About the ... Aflac is a member of the COG Pediatric Early Phase Clinical Trials Network (PEP-CTN), NANT, TACL ...

next page

Showing results 1-20

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

Clinical Trials Assistant information

See Decatur, GA salary details

$11

$19

$28

How much do clinical trials assistant jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for clinical trials assistant in Decatur, GA is $19.75, according to ZipRecruiter salary data. Most workers in this role earn between $16.20 and $22.79 per hour, depending on experience, location, and employer.

What are Clinical Trials Assistants?

Clinical Trials Assistants (CTAs) are professionals who support the planning, coordination, and administration of clinical trials, which are research studies that evaluate the safety and effectiveness of medical treatments or interventions. They handle tasks such as maintaining trial documentation, assisting with regulatory submissions, scheduling meetings, and ensuring data accuracy. CTAs play a crucial role in helping clinical research teams comply with protocols and regulatory requirements, making the clinical trial process run smoothly and efficiently.

How to become a clinical trials assistant?

To become a clinical trials assistant, candidates typically need a high school diploma or equivalent, with some roles preferring postsecondary education in health or science fields. Relevant skills include attention to detail, organization, and familiarity with clinical trial protocols and documentation. Gaining experience through internships or entry-level positions in healthcare or research settings can also improve job prospects.

What are some typical challenges a Clinical Trials Assistant faces during a study, and how can they be managed?

Clinical Trials Assistants often encounter challenges such as managing large volumes of documentation, ensuring timely data entry, and coordinating communication among multiple stakeholders. Staying organized and using established tracking systems can help manage documents efficiently. Proactive communication and regular check-ins with team members—such as study coordinators and data managers—are key to resolving issues quickly and maintaining study timelines. Embracing good time management practices and seeking mentorship from senior staff can further ease these common challenges.

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

AspectClinical Trials AssistantClinical Research Coordinator
CredentialsHigh school diploma or equivalent; some roles may require certificationBachelor’s degree in health sciences or related field; often requires certification
Work EnvironmentResearch sites, hospitals, clinics, pharmaceutical companiesResearch sites, hospitals, clinics, pharmaceutical companies
ResponsibilitiesAssist with data entry, document management, and trial logisticsOversee trial processes, patient recruitment, data collection, and compliance
Industry UsageCommonly used in clinical trial support rolesMore involved in trial management and coordination

While both roles support clinical trials, Clinical Trials Assistants focus on administrative and logistical tasks, whereas Clinical Research Coordinators handle more comprehensive trial management, patient interactions, and compliance activities.

How much money do clinical research assistants make?

Clinical research assistants typically earn a median annual salary of around $45,000 to $55,000, depending on experience, location, and the complexity of trials they support. Entry-level positions may start lower, while experienced assistants or those with specialized skills can earn higher wages. Salaries often increase with certifications and familiarity with clinical trial management tools.

What do clinical trial assistants do?

Clinical trial assistants support the coordination and management of clinical trials by handling documentation, scheduling, and communication between research teams and participants. They ensure compliance with protocols and regulatory requirements, often using trial management software, and may assist with data entry and tracking trial progress.

What qualifications do I need to be a clinical research assistant?

A clinical research assistant typically needs a high school diploma or equivalent, with some roles preferring a bachelor's degree in health sciences, biology, or a related field. Relevant skills include attention to detail, organizational abilities, and familiarity with clinical trial protocols and data management tools. Certification in Good Clinical Practice (GCP) or related training can also enhance job prospects.

What are the key skills and qualifications needed to thrive as a Clinical Trials Assistant, and why are they important?

To thrive as a Clinical Trials Assistant, you need a solid understanding of clinical research processes, regulatory guidelines, and attention to detail, often supported by a degree in life sciences. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is typically required. Strong organizational skills, effective communication, and the ability to multitask make candidates stand out in this role. These skills are essential for ensuring compliance, accurate documentation, and the smooth execution of clinical studies.
What are the most commonly searched types of Clinical Trials jobs in Decatur, GA? The most popular types of Clinical Trials jobs in Decatur, GA are:
What are popular job titles related to Clinical Trials Assistant jobs in Decatur, GA? For Clinical Trials Assistant jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Clinical Trials Assistant jobs in Decatur, GA look for? The top searched job categories for Clinical Trials Assistant jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Clinical Trials Assistant jobs? Cities near Decatur, GA with the most Clinical Trials Assistant job openings:
Clinical Trials Assistant jobs near you
Infographic showing various Clinical Trials Assistant job openings in Decatur, GA as of July 2026, with employment types broken down into 1% As Needed, 72% Full Time, 22% Part Time, 2% Temporary, and 3% Contract. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $41,084 per year, or $19.8 per hour.

Clinical Research Nurse

Denali Health

Atlanta, GA • On-site

Part-time, Per diem, Other

Posted 11 days ago

Job description

About Denali Health:
Denali Health is an Independent Research Organization (IRO) dedicated to accelerating the development of innovative therapies to market. We conduct Phase I-IV clinical trials across multiple therapeutic areas, including neurology, psychiatry, wound care, and other specialty areas. Our commitment to excellence in clinical research operations ensures the highest standards of patient care and scientific integrity.
Position Summary:
We are seeking an experienced Clinical Research Nurse to join our Atlanta team on a PRN basis. This position offers flexible scheduling while providing critical support to our clinical trial operations. The ideal candidate will have a strong foundation in clinical research nursing, excellent patient care skills, and the ability to work independently in a dynamic research environment.
Key Responsibilities:
  • Conduct patient screening, enrollment, and study visits according to protocol requirements
  • Perform clinical assessments, vital signs, phlebotomy, ECGs, and other study-related procedures
  • Administer investigational products and medications per protocol specifications
  • Ensure accurate and timely documentation in source documents and electronic data capture systems
  • Monitor patient safety and report adverse events in compliance with regulatory requirements
  • Educate patients and families about study procedures, informed consent, and expectations
  • Maintain regulatory compliance with FDA, ICH-GCP, and institutional guidelines
  • Coordinate with Principal Investigators, study coordinators, sponsors, and CROs
  • Assist with patient recruitment and retention activities
  • Maintain study supplies, equipment, and laboratory specimens

Required Qualifications:
  • Current Registered Nurse (RN) license in the State of Georgia
  • Minimum 1-2 years of clinical nursing experience
  • Valid BLS certification
  • Strong clinical assessment and procedural skills
  • Excellent communication and interpersonal abilities
  • Attention to detail and strong organizational skills
  • Ability to work independently and as part of a collaborative team
  • Proficiency with electronic medical records and data capture systems
  • Flexibility to work as needed based on study demands

Preferred Qualifications:
  • Previous clinical research experience
  • CCRP (Certified Clinical Research Professional) or ACRP certification
  • Experience with Phase I-IV clinical trials
  • Familiarity with ICH-GCP guidelines and FDA regulations
  • Phlebotomy certification
  • Experience in neurology, psychiatry, wound care, or specialty therapeutic areas
  • Bilingual capabilities (Spanish or other languages)

What We Offer:
  • Competitive PRN hourly rate
  • Flexible scheduling to accommodate your availability
  • Opportunity to work on cutting-edge clinical research
  • Exposure to diverse therapeutic areas and study phases
  • Professional development in clinical research
  • Collaborative and supportive work environment
  • Potential for increased hours based on the study pipeline

Physical Requirements:
  • Ability to stand and walk for extended periods
  • Manual dexterity for performing clinical procedures
  • Ability to lift up to 25 pounds
  • Visual acuity for detailed documentation and patient assessment

Note: This is a part-time position that requires working one week per month on-site according to the following schedule:
  • Tuesday - Friday: Night shift
  • Saturday - Sunday - Monday: Full-day shift (9:00 AM - 5:00 PM)

Please ensure you are available to commit to this schedule before applying.

Apply