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Vaccine Research Jobs in Decatur, GA (NOW HIRING)

CAMRIS International, LLC

Toxicologist

Atlanta, GA · On-site

Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS ...

CAMRIS International, LLC

Epidemiologist

Atlanta, GA · On-site

Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS ...

CAMRIS

Epidemiologist

Atlanta, GA · On-site

$105K - $140K/yr

Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS ...

CAMRIS

Environmental Health Scientist

Atlanta, GA · On-site

$115K - $145K/yr

Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS ...

CAMRIS

Toxicologist

Atlanta, GA · On-site

$110K - $145K/yr

Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS ...

CAMRIS

Toxicologist

Atlanta, GA · On-site

$110K - $145K/yr

Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS ...

CAMRIS

Environmental Health Scientist

Atlanta, GA · On-site

$115K - $145K/yr

Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS ...

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How much do vaccine research jobs pay per hour?

As of Sep 14, 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 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 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 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 September 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 Nurse

Decatur, GA • On-site

Alcanza Clinical Research
51 - 200 employees
Learn more about Alcanza Clinical Researchexternal

Full-time

Medical, Dental, Vision, Life, Retirement

Re-posted 7 days ago

Key responsibilities

  • Conduct clinical procedures such as venipunctures, injections, infusions, and other procedures according to study protocol and licensure.

  • Ensure the execution of assigned studies by performing tasks such as patient screening, consent, follow-up visits, data entry, and documentation.

  • Maintain study documentation, logs, and supplies, and assist with study start-up activities, site visits, and monitoring as needed.

Job description

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 Clinical Research Nurse works to ensure the execution of assigned studies, and performs clinical procedures, such as venipunctures, injections, prep or mixing of investigational study drugs and infusions, under the scope of the study protocol and in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs.

Key Responsibilities
Essential Job Duties: In collaboration with other members of the clinical research site team, works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:
  • Under the direction of the Site Manager/Director and the Principal/Sub Investigators, conducts the following according to study protocol, company processes & procedures, and in compliance with FDA, GCP, ICH regulations and guidelines: 
    • Screening of patients for study enrollment; 
    • Patient consents; 
    • Patient follow-up visits; 
    • Documenting in source clinic charts; 
    • Entering data in EDC and answers queries; 
    • Obtaining vital signs and ECGs; 
    • May 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; 
    • Performing procedures commensurate with licensure including vitals, ECGs/EKGs, venipunctures, injections, infusions, mixing drug and/or dispense investigational product; etc. 
    • Requesting and tracking medical record requests; 
    • Updating and maintaining logs, chart filings; 
    • Maintaining & ordering study specific supplies; 
    • Scheduling subjects for study visits and conducts appointment reminders; 
    • Building/updating source as needed; 
    • Conducting monitoring visits and resolves issues as needed in a timely manner; 
    • Ensuring study related reports and patient results are reviewed by investigator in a timely manner; 
o    Filing SAE/Deviation reports to Sponsor and IRB as needed;
o    Documenting and reporting adverse events;
o    Reporting non-compliance to appropriate staff in timely manner;
o    Maintaining positive and effective communication with clients and team members;
o    Always practicing ALCOAC principles with all documentation;
 
  • Be thoroughly familiar with the protocol, case report form, informed consent, source documentation, patient diary (when applicable), and study medication(s) for the assigned research study;
  • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
  • Prepare and attend site initiation visits (SIV’s) and Investigator Meetings (IMs), as needed;
  • May set up, train and maintain all technology needed for studies.
  • May assist with study recruitment, patient enrollment, and tracking as needed;
  • Maintaining confidentiality of patients, customers and company information, and;
  • Performing all other duties as requested or assigned. 

Skills, Knowledge and Expertise
Minimum Qualifications:  A Bachelor’s degree in Nursing (BSN) AND a minimum of 1 year of clinical experience, OR an equivalent combination of education and experience, is required.  An active, unrestricted RN license, in state of work location, is required.  BLS certification required.  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);
  • Proficiency with performing clinical procedures such as injections, vitals, EKGs, phlebotomy, infusions, etc. is required.  
  • 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.