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

Ensure copies/originals (as required) site documents are available for filing in the Trial Master ... Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. Good ...

Well-versed in clinical trial management. They are rigorous, detail-oriented, and precise in their reports. * Located in the US near a major airport. Ability to cover up to 65% regional travel.

Research Assistant

Atlanta, GA · On-site

$18.50 - $25.50/hr

... clinical trial. Your work helps ensure data is collected accurately, participants receive ... Support Clinical Research Visits: * Assist with participant visits and study-related procedures.

New

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 ...

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Clinical Trial Assistant information

See Decatur, GA salary details

$11

$36

$67

How much do clinical trial assistant jobs pay per hour?

As of Jun 27, 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.

Is CRA an entry-level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, monitoring, or related roles. Entry-level roles in clinical trials often include Clinical Trial Assistant or Clinical Research Coordinator, which can serve as stepping stones to a CRA position after gaining relevant skills and certifications. CRAs generally need a strong understanding of Good Clinical Practice (GCP) and may require a bachelor's degree in a health-related field.

How do I become a trial assistant?

To become a clinical trial assistant, candidates typically need a high school diploma or equivalent, with some roles preferring postsecondary education or relevant certifications. Experience in healthcare, research, or administrative support is beneficial, and familiarity with clinical trial protocols and data management tools can improve job prospects. Strong organizational skills and attention to detail are essential for success in this role.

What does a clinical trial assistant do?

A clinical trial assistant supports the management and coordination of clinical trials by preparing documentation, tracking study progress, and ensuring compliance with regulatory requirements. They often use specialized software and work closely with research teams, investigators, and sponsors to facilitate smooth trial operations.

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

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.

How to become a clinical trials assistant?

To become a clinical trial 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 processes, often supported by on-the-job training or certifications such as Good Clinical Practice (GCP). Experience in healthcare, research, or administrative roles can also improve job prospects in this field.

What are Clinical Trial Assistants?

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.
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:
Visiting Fellow - Clinical Research Fellow for the Division of Cardiothoracic Surgery

Visiting Fellow - Clinical Research Fellow for the Division of Cardiothoracic Surgery

Emory University

Atlanta, GA • On-site

Full-time

Medical

Posted 5 days ago


Emory Healthcare rating

7.7

Company rating: 7.7 out of 10

Based on 210 frontline employees who took The Breakroom Quiz

159th of 877 rated healthcare providers


Job description

Discover Your Career at Emory University
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 Division of Cardiothoracic Surgery at Emory University School of Medicine is seeking a highly motivated Clinical Research Fellow to join a dynamic and growing academic surgical research program. This fellowship is designed to provide comprehensive training in clinical research methodology, outcomes research, clinical trials, and translational investigation across the full spectrum of cardiothoracic surgery and cardiovascular disease.
This position offers an exceptional opportunity for surgical residents, medical graduates, or postdoctoral trainees interested in academic medicine, cardiothoracic surgery, cardiovascular research, or physician-scientist careers. The Fellow will work closely with faculty mentors on diverse clinical research initiatives spanning cardiac surgery, mechanical circulatory support, heart and lung transplantation, structural heart disease, extracorporeal support, surgical innovation, and outcomes research.
The fellowship provides structured mentorship, formal research training, and hands-on experience in clinical research design, execution, analysis, and dissemination.
Program Goals and Training Objectives
The Clinical Research Fellowship is designed to provide Fellows with:
  • Comprehensive training in clinical and translational research methodology
  • Experience with retrospective, prospective, and registry-based studies
  • Exposure to clinical trials, device development studies, and investigator-initiated protocols
  • Formal instruction in:
    • Biostatistics and statistical interpretation
    • Clinical research design and methodology
    • Manuscript writing and scientific communication
    • Grant preparation and funding strategies
    • Research ethics and regulatory compliance
    • Database management and analysis

A key longitudinal goal of the fellowship is to prepare trainees for academic careers and future roles as independent clinical investigators.
Research Environment and Opportunities
The Fellow will be embedded within a highly productive academic cardiothoracic surgery research environment with access to:
  • Large institutional clinical databases and electronic health record-derived research data warehouses
  • National clinical registries including STS, UNOS, SRTR, CMS, and administrative datasets
  • Clinical trial infrastructure supporting investigator-initiated and industry-sponsored studies
  • Multicenter registry collaborations
  • Translational and device-related clinical research initiatives
  • Opportunities to participate in innovation and surgical device development

The Fellow will work directly with faculty mentors and collaborate with multidisciplinary teams including surgeons, cardiologists, intensivists, biostatisticians, engineers, and research coordinators.
Research areas include, but are not limited to:
  • Outcomes research in cardiothoracic surgery
  • Mechanical circulatory support (LVAD, RVAD, ECMO)
  • Heart and lung transplantation
  • Structural heart and valve interventions
  • Surgical innovation and device-related clinical research
  • Health services and policy research

Registry-based outcomes and comparative effectiveness research
Fellow Responsibilities
The Clinical Research Fellow will:
  • Design and conduct clinical research studies
  • Perform data collection, management, and analysis
  • Lead and contribute to manuscript preparation and publication
  • Present research findings at national and international scientific meetings
  • Assist in clinical trial development and execution
  • Participate in research meetings, journal clubs, and academic conferences
  • Contribute to grant preparation and regulatory submissions (IRB, protocols)
  • Participate in seeking out federal, local and society cardiothoracic related research application opportunities

Fellows are expected to develop independent research projects under faculty mentorship.
Mentorship Structure
The Fellow will be supervised by a dedicated faculty mentor team consisting of experienced clinical investigators with active research programs and national leadership in cardiothoracic surgery research.
Mentorship will include:
  • Weekly one-on-one research mentorship meetings
  • Structured project planning and progress review
  • Career development guidance
  • Opportunities for national collaboration and networking

Duration and Time Commitment
  • Full-time position (minimum 40 hours per week)
  • Typical duration: 1-2 years
  • Start date: Flexible (rolling start dates available)

Qualifications
Required Qualifications
Applicants must have one of the following:
  • M.D., D.O., or equivalent medical degree
  • Ph.D. or equivalent doctoral degree
  • Enrollment in or completion of a surgical residency or medical training program
  • Must demonstrate ability to effectively communicate in written and spoken English sufficient for clinical research activities, regulatory documentation and/or interdisciplinary collaboration.

Preferred candidates include:
  • Surgical residents pursuing dedicated research time
  • Medical graduates interested in cardiothoracic surgery or cardiovascular research
  • Postdoctoral trainees interested in academic careers
  • Individuals interested in clinical research, academic medicine, or physician-scientist career pathways

Expected Academic Outcomes
Fellows are expected to:
  • Publish multiple peer-reviewed manuscripts
  • Present research at national scientific meetings
  • Develop skills in clinical research methodology
  • Build a foundation for academic or physician-scientist careers

Institutional Environment
Emory University Hospital and Emory Healthcare represent one of the leading academic medical centers in the United States, with a large volume of advanced cardiac and thoracic surgical procedures and a strong commitment to academic excellence, innovation, and research.
The Division of Cardiothoracic Surgery offers a highly collaborative and supportive academic environment with extensive infrastructure supporting clinical, translational, and outcomes research.
Compensation and Benefits
  • Competitive salary (commensurate with experience)
  • Health insurance and institutional benefits
  • Funding support for national conference presentation
  • Structured mentorship and academic career development

Application Instructions
Interested applicants should submit:
  • Curriculum vitae (CV)
  • Personal statement describing research interests and career goals
  • Names and contact information for 2-3 references

Applications will be reviewed on a rolling basis until positions are filled.
NOTE: This role will be granted the opportunity to work from home regularly but must be able to commute to Emory University on a flexible weekly schedule based upon business needs. Schedule is based on agreed upon guidelines of department. This role requires residency in the state of GA. Emory reserves the right to change remote work 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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