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Adverse Event Jobs in Georgia (NOW HIRING)

YO AI Labs

Hematology Expert - Remote

Atlanta, GA · Remote

$150 - $200/hr

Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution, and patient safety narratives. * Review benefit-risk assessments and identify clinically inconsistent ...

YO AI Labs

Oncology Expert - Remote

Atlanta, GA · Remote

$150 - $200/hr

Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution, and patient safety narratives. * Review benefit-risk assessments and identify clinically inconsistent ...

YO AI Labs

Clinicia Expert - Remote

Atlanta, GA · Remote

$150 - $200/hr

Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution, and patient safety narratives. * Review benefit-risk assessments and identify clinically inconsistent ...

Fox Theatre, Inc.

Event Staff

Atlanta, GA · On-site

$15.50/hr

Event Staff provides all guests with a positive, lasting impression of the Fox Theatre by ... Must be able to work outside, in adverse weather conditions; * Must be Resolution Oriented and ...

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Adverse Event information

What is an adverse event?

An Adverse Event (AE) refers to any undesirable experience or medical occurrence in a patient or clinical trial participant who has been given a pharmaceutical product or is undergoing medical treatment. These events can range from mild side effects to serious health complications and may or may not be directly caused by the treatment itself. Monitoring and reporting adverse events are essential for ensuring patient safety and for regulatory compliance in clinical research. Identifying and documenting AEs helps healthcare professionals assess risks and benefits of medications or treatments and can lead to changes in prescribing information or regulatory actions.

What are the key skills and qualifications needed to thrive as a pharmacovigilance (adverse event) specialist?

To thrive as a Pharmacovigilance (Adverse Event) Specialist, you need a background in life sciences or pharmacy, knowledge of regulatory guidelines, and experience in drug safety reporting. Familiarity with safety databases such as Argus or ArisG, as well as understanding of MedDRA coding and ICH-GCP standards, is typically required. Attention to detail, analytical thinking, and strong communication skills help specialists accurately assess and report adverse events. These competencies are crucial for ensuring patient safety, regulatory compliance, and effective risk management in pharmaceutical settings.

What are common challenges faced by professionals working in adverse event reporting, and how can they be managed?

Professionals in Adverse Event reporting often encounter challenges such as tight regulatory deadlines, the need for meticulous attention to detail, and effective communication with cross-functional teams like clinical, safety, and regulatory affairs. Managing a high volume of reports while ensuring accuracy and compliance can be demanding. To address these challenges, it's important to develop strong organizational skills, stay current on regulatory changes, and build collaborative relationships within your organization. Leveraging technology and standardized processes also helps streamline reporting and ensure timely submissions.

What is the difference between Adverse Event vs Clinical Research Coordinator?

AspectAdverse EventClinical Research Coordinator
Required credentialsMedical knowledge, pharmacovigilance trainingResearch ethics, study protocols
Work environmentHealthcare settings, hospitals, clinicsResearch sites, hospitals, clinics
Employer and industry usagePharmaceutical companies, healthcare providersResearch institutions, hospitals
Common search intentUnderstanding safety reportingManaging clinical trials

Adverse Event involves monitoring and reporting negative effects related to medical treatments, requiring medical and pharmacovigilance expertise. Clinical Research Coordinators manage and oversee clinical trials, focusing on study procedures and participant coordination. While both roles operate within healthcare and research environments, their responsibilities and required skills differ significantly.

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

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

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

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

Adverse Event jobs near you
Infographic showing various Adverse Event job openings in Georgia as of August 2026, with employment types broken down into 76% Full Time, 19% Part Time, and 5% Temporary. Highlights an 100% In-person job distribution.

Pharmacy Quality & Safety Program Manager

Curant Health

Smyrna, GA • On-site

$64.75 - $76.25/hr

Full-time

Posted 19 days 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