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Adverse Event Reporting Jobs in Georgia (NOW HIRING)

Denali Health

Nurse Practitioner

Atlanta, GA · On-site

Counsel participants on study procedures, investigational products, and adverse-event reporting * Manage and document AEs/SAEs, escalating to PI and sponsor as required * Maintain GCP-compliant ...

Denali Health

Nurse Practitioner

Atlanta, GA · On-site

Counsel participants on study procedures, investigational products, and adverse-event reporting * Manage and document AEs/SAEs, escalating to PI and sponsor as required * Maintain GCP-compliant ...

Lukos

VAERS Clinician

Atlanta, GA · On-site

The Vaccine Adverse Event Reporting System (VAERS) is a mandated program sponsored jointly by the Centers for Disease Control and Prevention (CDC) and the US Food and Drug Administration (FDA). The ...

Lukos

VAERS Clinician

Atlanta, GA · On-site +1

The Vaccine Adverse Event Reporting System (VAERS) is a mandated program sponsored jointly by the Centers for Disease Control and Prevention (CDC) and the US Food and Drug Administration (FDA). The ...

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How much do adverse event reporting jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for adverse event reporting in Georgia is $21.62, according to ZipRecruiter salary data. Most workers in this role earn between $18.89 and $24.13 per hour, depending on experience, location, and employer.

What is adverse event reporting?

An Adverse Event Reporting job involves monitoring, documenting, and reporting adverse events related to medical products, such as drugs, devices, or vaccines. Professionals in this role collect data from healthcare providers, patients, and clinical trials to ensure compliance with regulatory requirements. They analyze reports to assess potential safety concerns and work with regulatory agencies like the FDA or EMA. Their primary goal is to ensure patient safety by identifying and mitigating risks associated with medical products.

What are the typical challenges faced in an adverse event reporting role?

Professionals in Adverse Event Reporting often handle large volumes of complex data that require careful evaluation and timely submission to regulatory authorities. One common challenge is staying up to date with ever-changing regulations and ensuring that all reports meet stringent compliance standards. Additionally, working across multiple teams—such as clinical, regulatory, and quality assurance—requires excellent coordination and communication skills. Being detail-oriented and proactive helps in identifying potential issues early and maintaining high-quality, compliant documentation.

What are the key skills and qualifications needed to thrive in the adverse event reporting position, and why are they important?

To thrive in Adverse Event Reporting, you need a solid background in life sciences or healthcare, attention to detail, and a clear understanding of regulatory requirements. Familiarity with pharmacovigilance databases, safety monitoring systems, and relevant certifications such as those from the Drug Information Association (DIA) or Regulatory Affairs Certification (RAC) is valuable. Strong analytical thinking, written communication skills, and the ability to work collaboratively across departments are valuable soft skills. These qualifications ensure accurate, reliable reporting and compliance with industry regulations, which is crucial for patient safety and effective risk management.

What are the most commonly searched types of Adverse Event Reporting jobs in Georgia?

The most popular types of Adverse Event Reporting jobs in Georgia are:

What are popular job titles related to Adverse Event Reporting jobs in Georgia?

For Adverse Event Reporting jobs in Georgia, the most frequently searched job titles are:

What job categories do people searching Adverse Event Reporting jobs in Georgia look for?

The top searched job categories for Adverse Event Reporting jobs in Georgia are:

Adverse Event Reporting jobs near you
Infographic showing various Adverse Event Reporting job openings in Georgia as of August 2026, with employment types broken down into 88% Full Time, and 12% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $44,967 per year, or $21.6 per hour.

Pharmacy Quality & Safety Program Manager

Smyrna, GA • On-site

Curant Health
Health Care and Social Assistance • 51 - 200 employees
Learn more about Curant Healthexternal

$64.75 - $76.25/hr

Full-time

Re-posted 2 hours ago

Job description

Join Curant Health

Curant Health is seeking an experienced Pharmacy Quality & Safety Program Manager to lead medication safety and quality initiatives across the organization. This role serves as the subject matter expert for medication safety, pharmacovigilance, adverse drug event reporting, product complaints, deviation investigations, and CAPA management to improve patient outcomes and reduce medication-related risk.

This is an individual contributor role that partners closely with Pharmacy Operations, healthcare providers, pharmaceutical manufacturers, and cross-functional teams to drive continuous quality improvement.

Key Responsibilities
  • Lead medication safety, adverse event reporting, product complaint management, and pharmacovigilance activities.
  • Conduct investigations, root cause analyses, deviation reporting, and CAPA development.
  • Analyze safety trends and implement process improvements to enhance patient outcomes.
  • Develop and maintain policies, procedures, and quality documentation.
  • Support manufacturer-sponsored safety programs and contractual reporting requirements.
  • Prepare reports, dashboards, and presentations for leadership and stakeholders.
  • Serve as a medication safety resource for pharmacy teams while promoting a culture of quality and continuous improvement.
Qualifications
  • PharmD or Bachelor's degree in Pharmacy with an active, unrestricted pharmacist license.
  • Dual licensure in Florida and Georgia, or the ability to obtain both.
  • Five or more years of pharmacy experience, preferably in a specialty or mail-order setting.
  • Three or more years of experience in medication safety, pharmacovigilance, adverse event reporting, product complaints, deviations, CAPA, or pharmacy quality.
  • Strong knowledge of medication safety, investigations, root cause analysis, HIPAA, and quality improvement.
  • Excellent communication, collaboration, analytical, and project management skills.
  • Proficiency with Microsoft Word, Excel, and PowerPoint.
Why Curant Health?

Join a team dedicated to improving patient outcomes through innovative pharmacy care while helping shape and strengthen our medication safety and quality programs.

Apply today to make a meaningful impact on patient safety at Curant Health.

Apply