Required Minimum Experience: * 2 years or more of experience in nursing and/or adverse event monitoring, remediation, and problem solving. Required Minimum Skills: * Computer skills required to ...
Required Minimum Experience: * 2 years or more of experience in nursing and/or adverse event monitoring, remediation, and problem solving. Required Minimum Skills: * Computer skills required to ...
Required Minimum Experience: * 2 years or more of experience in nursing and/or adverse event monitoring, remediation, and problem solving. Required Minimum Skills: * Computer skills required to ...
Required Minimum Experience: * 2 years or more of experience in nursing and/or adverse event monitoring, remediation, and problem solving. Required Minimum Skills: * Computer skills required to ...
Required Minimum Experience: * 2 years or more of experience in nursing and/or adverse event monitoring, remediation, and problem solving. Required Minimum Skills: * Computer skills required to ...
Required Minimum Experience: * 2 years or more of experience in nursing and/or adverse event monitoring, remediation, and problem solving. Required Minimum Skills: * Computer skills required to ...
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 ...
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 ...
Cardiology Research Data Specialist, Gwinnett Hub
Lawrenceville, GA · On-site
$60 - $80/hr
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Cardiology Research Data Specialist, Gwinnett Hub
Lawrenceville, GA · On-site
$60 - $80/hr
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Cardiology Research Data Specialist, Gwinnett Hub
Lawrenceville, GA · On-site
$60 - $80/hr
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Cardiology Research Data Specialist, Gwinnett Hub
Lawrenceville, GA · On-site
$60 - $80/hr
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...
Responsible for addressing and acting on adverse events and action thresholds in collaboration with facility management. * Maintains integrity of medical records and other organization administrative ...
Responsible for addressing and acting on adverse events and action thresholds in collaboration with facility management. * Maintains integrity of medical records and other organization administrative ...
Registered Nurse Surgery Center
Augusta, GA · On-site
$60 - $80/hr
Responsible for addressing and acting on adverse events and action thresholds in collaboration with facility management.* Maintains integrity of medical records and other organization administrative ...
Registered Nurse Surgery Center
Augusta, GA · On-site
$60 - $80/hr
Responsible for addressing and acting on adverse events and action thresholds in collaboration with facility management.* Maintains integrity of medical records and other organization administrative ...
Registered Nurse Per Diem
Augusta, GA · On-site
Responsible for addressing and acting on adverse events and action thresholds in collaboration with facility management. * Maintains integrity of medical records and other organization administrative ...
Registered Nurse Per Diem
Augusta, GA · On-site
Responsible for addressing and acting on adverse events and action thresholds in collaboration with facility management. * Maintains integrity of medical records and other organization administrative ...
Per Diem Registered Nurse
Decatur, GA · On-site
Responsible for addressing and acting on adverse events and action thresholds in collaboration with facility management. * Maintains integrity of medical records and other organization administrative ...
Per Diem Registered Nurse
Decatur, GA · On-site
Responsible for addressing and acting on adverse events and action thresholds in collaboration with facility management. * Maintains integrity of medical records and other organization administrative ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
VAERS Clinician
Atlanta, GA · On-site
$52K - $69K/yr
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 ...
VAERS Clinician
Atlanta, GA · On-site
$52K - $69K/yr
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 ...
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?
| Aspect | Adverse Event | Clinical Research Coordinator |
|---|---|---|
| Required credentials | Medical knowledge, pharmacovigilance training | Research ethics, study protocols |
| Work environment | Healthcare settings, hospitals, clinics | Research sites, hospitals, clinics |
| Employer and industry usage | Pharmaceutical companies, healthcare providers | Research institutions, hospitals |
| Common search intent | Understanding safety reporting | Managing 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:
Other
Posted 5 days ago
Wellstar Health System rating
7.4
Based on 357 frontline employees who took The Breakroom Quiz
263rd of 898 rated healthcare providers
Job description
How would you like to work in a place where your contributions and ideas are valued? A place where you can serve with compassion, pursue excellence and honor every voice? At Wellstar, our mission is simple, yet powerful: to enhance the health and well-being of every person we serve. We are proud to have become a shining example of what's possible when the brightest professionals dedicate themselves to making a difference in the healthcare industry, and in people's lives.
Work Shift
Day (United States of America)Job Summary:Coordinates the patient safety programs at Wellstar. Gathers data detailing patient-related errors and conducts causal analysis to include Root Cause Analysis (RCAs). Conducts risk assessments based on ECRI recommendations, recommends practice changes, policies or programs that could mitigate risks and enhance Wellstar's culture of safety. Participates in organization development and provides patient safety and risk reduction training events.
Required Minimum Education:
- Associate's degree in Nursing
Required Minimum License(s) and Certification(s):
- Current Registered Nursing license in Georgia or qualifying multi-state compact license.
- All certifications are required upon hire unless otherwise stated.
- 2 years or more of experience in nursing and/or adverse event monitoring, remediation, and problem solving.
- Computer skills required to include Microsoft Word Excel and PowerPoint
- Demonstrated excellence in interpersonal and written communication
- Group facilitation skills and ability to manage programs and projects
- Bachelor's degree in nursing
- 4 years or more of experience in nursing and Healthcare Quality or Patient Safety/Risk Management
- Experience with process improvement concepts and tools and data management
- CPHQ or CPPS certification
Join us and discover the support to do more meaningful workâ€"and enjoy a more rewarding life. Connect with the most integrated health system in Georgia, and start a future that gives you more.
What Wellstar Health System employees say
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About WellStar Health System
Sourced by ZipRecruiter
Wellstar Health System is a leading non-profit health organization based in Marietta, GA, US. Operating in the fast-growing sector of healthcare, the company specializes in providing a wide array of medical services, including emergency care, diagnostic imaging, maternity services, and several others. The welkin of Wellstar Health System dates back to 1993 when it emerged into being. The company thrives on its core values of compassion, accountability, respect, integrity, and excellence to deliver its mission of enhancing the health and well-being of every person it serves.
Industry
Health care and social assistance and outpatient health care
Company size
10,000+ Employees
Headquarters location
Marietta, GA, US