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

As a Clinical Research Assistant, PRN , you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life.

As a Clinical Research Assistant, PRN , you'll play a key role in delivering life-changing research opportunities to participants but with the flexibility to work when and where it fits your life.

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 ...

Clinical Research Coordinator

Decatur, GA

$23.75 - $31.50/hr

The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in ... May assist with study recruitment, patient enrollment, and tracking as needed; * Maintaining ...

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Clinical Research Assistant information

See Decatur, GA salary details

$7

$22

$45

How much do clinical research assistant jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for clinical research assistant in Decatur, GA is $22.17, according to ZipRecruiter salary data. Most workers in this role earn between $16.88 and $25.34 per hour, depending on experience, location, and employer.

What are Clinical Research Assistants?

Clinical Research Assistants are professionals who support clinical research studies by performing a range of administrative and research-related tasks. They help collect and manage data, assist with patient recruitment, prepare study materials, and ensure compliance with research protocols and regulations. Their work is crucial in advancing medical knowledge and ensuring that clinical trials run smoothly and ethically. Clinical Research Assistants often work under the supervision of principal investigators or clinical research coordinators in hospitals, universities, or pharmaceutical companies.

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

To thrive as a Clinical Research Assistant, you need a bachelor’s degree in a life science or health-related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and good clinical practice (GCP) certification are typically required. Excellent communication, teamwork, and problem-solving abilities help you excel in coordinating with research teams and participants. These skills ensure accurate data collection, regulatory compliance, and the smooth execution of clinical studies.

What Does a Clinical Research Assistant Do?

A clinical research assistant—or clinical research associate (CRA)—helps lead researchers during clinical trials for new drugs and medical devices. As a clinical research assistant, your responsibilities include preparing the laboratory, processing volunteers, taking biological samples or vital signs, and organizing data. You may also be required to set up and clean work areas. Your job is to assist the researchers in any way possible, helping them conduct sound, ethical, and scientifically accurate research.

What are some common challenges Clinical Research Assistants face when coordinating multiple studies simultaneously?

Clinical Research Assistants often manage several studies at once, which can lead to challenges in balancing competing deadlines, maintaining accurate documentation, and ensuring compliance with complex protocols. Effective time management and organizational skills are crucial to handle overlapping tasks such as scheduling patient visits, collecting data, and preparing regulatory submissions. Collaborating closely with principal investigators, coordinators, and other team members helps distribute the workload and maintain research quality. Developing strong communication habits and utilizing digital tracking tools can further streamline workflow and reduce errors.

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

AspectClinical Research AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; certifications like CCRP are a plusRequires a bachelor's degree; certifications such as CCRP or CCRC are common
Work EnvironmentAssists in data collection, patient scheduling, and administrative tasks in clinical trial settingsManages study protocols, patient recruitment, and regulatory compliance in clinical trial sites
Employer & IndustryHospitals, research institutions, pharmaceutical companiesHospitals, research centers, pharmaceutical companies

Both roles support clinical research but differ in responsibilities. Clinical Research Assistants focus on data collection and administrative tasks, while Clinical Research Coordinators oversee study management and patient interactions. Understanding these differences helps in choosing the right career path or job search focus.

What are the most commonly searched types of Clinical Research jobs in Decatur, GA? The most popular types of Clinical Research jobs in Decatur, GA are:
What are popular job titles related to Clinical Research Assistant jobs in Decatur, GA? For Clinical Research Assistant jobs in Decatur, GA, the most frequently searched job titles are:
What cities near Decatur, GA are hiring for Clinical Research Assistant jobs? Cities near Decatur, GA with the most Clinical Research Assistant job openings:

Clinical Research Assistant

Metro Infectious Disease Consultants

Decatur, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Job description

Metro Infusion Center/Metro Infectious Disease Consultants is seeking a Full-Time Clinical Research Assistant who will be responsible for providing non-clinical support in the operations and monitoring of clinical trials. The Research Assistant will analyze and evaluate clinical data gathered during research while ensuring compliance with protocols and overall clinical objectives. Responsibilities assigned to individuals can and will change at any time at the discretion of management or the supervisor

Schedule: Monday-Friday 8:30am-5:00 pm, in-person

Duties:

  • Enter data proficiently and accurately into a data capture system for sponsors and contract research organizations to monitor.
  • Request or acquire the equipment and supplies necessary for each project.
  • Set up, calibrate, and maintain laboratory and/or field research equipment, as specified by the requirements of the study.
  • Assist Clinical Research Associates that are monitoring each study (on and off-site).
  • Invoice for payments associated with the clinical trial budget.
  • Ship lab samples while following regulations and protocols when needed.
  • Attend project meetings and communicate with fellow staff through email and phone calls.
  • Perform ECG's
  • Upload study documents to EMR chart
  • Track specimen shipments
  • Responsibilities may evolve depending on protocol specific requirements

Requirements

  • High school diploma required
  • Bachelor's Degree preferred
  • Proof of current vaccinations, including recommended boosters, commonly required for those working with immunocompromised patients, including measles, mumps, rubella, varicella, hepatitis A & B, influenza.

Requests for accommodations/exceptions will be considered on a case-by-case basis, consistent with applicable laws.

Benefits

  • 401(k)
  • Dental insurance
  • Health insurance
  • Life insurance
  • Paid time off
  • Referral program
  • Vision insurance
  • $50,000-$53,000 ($20/hour + monthly bonus)