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Vaccine Research Jobs in Decatur, GA (NOW HIRING)

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How much do vaccine research jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for vaccine research in Decatur, GA is $21.70, according to ZipRecruiter salary data. Most workers in this role earn between $16.88 and $23.22 per hour, depending on experience, location, and employer.

What are the typical daily responsibilities of a vaccine research professional?

Professionals in vaccine research spend their days designing and conducting laboratory experiments, analyzing immunological or clinical data, and documenting their findings for reports or publications. They often work closely with other scientists, clinicians, and regulatory specialists to ensure research aligns with safety standards and research protocols. Collaboration and frequent communication within interdisciplinary teams are common, as is attending meetings to discuss progress or adapt research strategies. Additionally, those in this field may participate in grant writing, presenting at conferences, or staying updated with the latest scientific advancements. These varied responsibilities contribute to a dynamic and intellectually stimulating work environment.

What is a vaccine research job?

A Vaccine Research job involves studying and developing vaccines to prevent infectious diseases. Professionals in this field conduct laboratory experiments, clinical trials, and data analysis to ensure vaccine safety and effectiveness. They work in pharmaceutical companies, government agencies, or academic institutions. Their goal is to create new vaccines or improve existing ones to protect public health.

What are the key skills and qualifications needed to thrive in vaccine research?

A career in Vaccine Research requires a strong background in immunology, microbiology, and molecular biology, often supported by an advanced degree such as a Ph.D. or M.Sc. in a related field. Experience with laboratory techniques, data analysis software, and familiarity with regulatory compliance and Good Laboratory Practice (GLP) certifications are highly valuable. Critical thinking, attention to detail, and excellent collaboration skills enable researchers to effectively design experiments and communicate findings within multidisciplinary teams. These competencies ensure robust scientific outcomes, safety in clinical trials, and the successful development of vaccines that address public health needs.

What are popular job titles related to Vaccine Research jobs in Decatur, GA? For Vaccine Research jobs in Decatur, GA, the most frequently searched job titles are:
What job categories do people searching Vaccine Research jobs in Decatur, GA look for? The top searched job categories for Vaccine Research jobs in Decatur, GA are:
What cities near Decatur, GA are hiring for Vaccine Research jobs? Cities near Decatur, GA with the most Vaccine Research job openings:
Vaccine Research jobs near you
Infographic showing various Vaccine Research job openings in Decatur, GA as of August 2026, with employment types broken down into 33% Full Time, and 67% Part Time. Highlights an 100% In-person job distribution, with an average salary of $45,128 per year, or $21.7 per hour.

Clinical Research Assistant

Alcanza Clinical Research

Decatur, GA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 12 days ago

Job description

Clinical Research Assistant
Department: Operations
Employment Type: Full Time
Location: Accel Research Sites - Decatur, GA
Reporting To: Benoit Tete
Description
Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in AL, AZ, FL, GA, IL, MA, MI, MO, NV, VA, SC, TN, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.
The Research Assistant (RA) provides support to the Clinical Research Coordinators (CRCs), Site Manager, Principal and Sub Investigators, and other site staff in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. The RA performs clinical, lab, and administrative tasks as needed for the successful operation of the clinical research site.
Key Responsibilities
Essential Job Duties: In collaboration with other members of the clinical research site team, assists with the execution of assigned studies, and support functions as needed. Responsibilities may include but are not limited to:
  • Under the direction of the Site Manager/Director and the Principal/Sub Investigators, assists the CRCs and other site staff in their responsibilities by conducting the following according to study protocol:
    • Assists with the basic screening of patients for study enrollment;
    • Assists with patient follow-up visits;
    • Documents in source clinic charts;
    • Enters data in EDC and answers queries;
    • Obtains vital signs and ECGs;
    • May perform blood draws;
    • Perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
    • Request and track medical record requests;
    • Enters data in EDC and answers queries;
    • Assists the CRC with updating and maintaining logs and filing in charts, and with chart filing; and
    • Schedules subjects for study visits, conducts appointment reminders, and reschedules visits if needed;
  • Ensures study related reports and patient results are reviewed by the Research Coordinator and/or investigator in a timely manner.
  • Assists the CRC and/or Manager with study recruitment, patient enrollment, and tracking as needed;
  • Maintains strict confidentiality of patients, employees, customers and company information at all times and adheres to HIPAA Guidelines; and
  • Perform all other duties as requested or assigned.

Skills, Knowledge and Expertise
Minimum Qualifications: A High School diploma and 1 year of administrative / clinical experience is required. 1 year or more years of clinical research or clinical experience is preferred. Bi-lingual (English / Spanish) proficiency is a plus.
Required Skills:
  • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40+ wpm).
  • Must possess strong organizational skills and attention to detail.
  • Well-developed written and verbal communication skills.
  • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
  • Ability to effectively handle multiple tasks and adapt to changes in workloads and priorities.
  • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
  • Must possess a high degree of integrity and dependability.
  • Ability to work under minimal supervision, identify problems and implement solutions.
  • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

Benefits
  • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
  • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.

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