Adverse Event Reporting Officer
$17 - $21.50/hr
The Adverse Event Reporting Officer (AERO) is responsible for reporting product safety events to our clients, maintaining appropriate records, and assisting with internal audits. The key ...
$17 - $21.50/hr
The Adverse Event Reporting Officer (AERO) is responsible for reporting product safety events to our clients, maintaining appropriate records, and assisting with internal audits. The key ...
$17 - $21.50/hr
The Adverse Event Reporting Officer (AERO) is responsible for reporting product safety events to our clients, maintaining appropriate records, and assisting with internal audits. The key ...
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize quality, efficiency & productivity in systems throughout TMC and other Terumo facilities by MDR ...
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize quality, efficiency & productivity in systems throughout TMC and other Terumo facilities by MDR ...
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize quality, efficiency & productivity in systems throughout TMC and other Terumo facilities by MDR ...
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize quality, efficiency & productivity in systems throughout TMC and other Terumo facilities by MDR ...
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize quality, efficiency & productivity in systems throughout TMC and other Terumo facilities by MDR ...
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize quality, efficiency & productivity in systems throughout TMC and other Terumo facilities by MDR ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Mundelein, IL · On-site
$67K - $101K/yr
Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...
Niles, IL · On-site
Manage and oversee adverse event reporting programs for OTC drug products, dietary supplements, cosmetics, and medical devices in accordance with FDA requirements. * Evaluate consumer complaints ...
Niles, IL · On-site
Manage and oversee adverse event reporting programs for OTC drug products, dietary supplements, cosmetics, and medical devices in accordance with FDA requirements. * Evaluate consumer complaints ...
Moundsview, MN · On-site
$24 - $27/hr
Process Medical Device Reports (MDRs) and adverse event cases * Maintain accurate complaint and vigilance records * Analyze safety and clinical data for reporting purposes * Ensure compliance with ...
Quick apply
Moundsview, MN · On-site
$24 - $27/hr
Process Medical Device Reports (MDRs) and adverse event cases * Maintain accurate complaint and vigilance records * Analyze safety and clinical data for reporting purposes * Ensure compliance with ...
Manage and oversee adverse event reporting programs for OTC drug products, dietary supplements, cosmetics, and medical devices in accordance with FDA requirements. * Evaluate consumer complaints ...
Manage and oversee adverse event reporting programs for OTC drug products, dietary supplements, cosmetics, and medical devices in accordance with FDA requirements. * Evaluate consumer complaints ...
... adverse event reporting process. 3. Analyzes and makes recommendations regarding complaints received by Merit to determine if they are reportable to global regulatory bodies. 4. Participates in ...
... adverse event reporting process. 3. Analyzes and makes recommendations regarding complaints received by Merit to determine if they are reportable to global regulatory bodies. 4. Participates in ...
Experience with medical device global adverse event reporting required, such as MDR, MPR, and Vigilance, TGA, etc. Self-motivated, self-directing, strong attention to detail and excellent time ...
Experience with medical device global adverse event reporting required, such as MDR, MPR, and Vigilance, TGA, etc. Self-motivated, self-directing, strong attention to detail and excellent time ...
Moundsview, MN · On-site
$28 - $31/hr
Manage adverse event reporting. * Monitor medical device surveillance. * Maintain MDR and ADE records. * Review clinical safety data. * Prepare safety summaries and reports. * Ensure regulatory ...
Quick apply
Moundsview, MN · On-site
$28 - $31/hr
Manage adverse event reporting. * Monitor medical device surveillance. * Maintain MDR and ADE records. * Review clinical safety data. * Prepare safety summaries and reports. * Ensure regulatory ...
Initiates, owns, or assists with internal audit and CAPA actions as they relate to complaint records and/or adverse event reporting * Participates in complaint record remediation planning and ...
Initiates, owns, or assists with internal audit and CAPA actions as they relate to complaint records and/or adverse event reporting * Participates in complaint record remediation planning and ...
Manage adverse event reporting. * Monitor medical device surveillance. * Maintain MDR and ADE records. * Review clinical safety data. * Prepare safety summaries and reports. * Ensure regulatory ...
Manage adverse event reporting. * Monitor medical device surveillance. * Maintain MDR and ADE records. * Review clinical safety data. * Prepare safety summaries and reports. * Ensure regulatory ...
Moundsview, MN · On-site
$25 - $30/hr
Manage adverse event reporting. * Monitor medical device surveillance. * Maintain MDR and ADE records. * Review clinical safety data. * Prepare safety summaries and reports. * Ensure regulatory ...
Quick apply
Moundsview, MN · On-site
$25 - $30/hr
Manage adverse event reporting. * Monitor medical device surveillance. * Maintain MDR and ADE records. * Review clinical safety data. * Prepare safety summaries and reports. * Ensure regulatory ...
California, MO · On-site
$70 - $100/hr
Maintains appropriate records for the Global Quality Assurance adverse event reporting system as defined in relevant procedures. * Prepares for, participates in and assists with FDA facility ...
California, MO · On-site
$70 - $100/hr
Maintains appropriate records for the Global Quality Assurance adverse event reporting system as defined in relevant procedures. * Prepares for, participates in and assists with FDA facility ...
$11.54 - $13.92
9% of jobs
$13.92 - $16.30
0% of jobs
$16.30 - $18.68
0% of jobs
$18.68 - $21.07
12% of jobs
$21.39 is the 25th percentile. Wages below this are outliers.
$21.07 - $23.45
25% of jobs
The median wage is $24.04 / hr.
$23.45 - $25.83
14% of jobs
$28.01 is the 75th percentile. Wages above this are outliers.
$25.83 - $28.21
15% of jobs
$28.21 - $30.59
6% of jobs
$30.59 - $32.98
0% of jobs
$32.98 - $35.36
12% of jobs
$35.36 - $37.74
5% of jobs
$11
$25
$37
| Aspect | Temporary Adverse Event Reporting | Pharmacovigilance Associate |
|---|---|---|
| Credentials | Typically requires healthcare or life sciences background, certifications vary | Requires similar healthcare or life sciences background, often with pharmacovigilance certifications |
| Work Environment | Often in clinical settings, healthcare facilities, or pharmaceutical companies | Primarily in pharmaceutical companies, CROs, or regulatory agencies |
| Industry Usage | Used during clinical trials or post-market surveillance for reporting adverse events temporarily | Ongoing role in monitoring, analyzing, and reporting adverse events in drug safety |
Temporary Adverse Event Reporting involves short-term documentation of adverse events, often during clinical trials or specific studies. Pharmacovigilance Associates handle continuous monitoring and analysis of adverse events for drug safety. While both roles require similar backgrounds, their scope and duration differ significantly.
Cities with the most Temporary Adverse Event Reporting job openings:
The most popular types of Adverse Event Reporting jobs are:
States with the most job openings for Temporary Adverse Event Reporting jobs include:
Agency:
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Compliance and RegulatoryJob Description:
JOB SUMMARY:Omnicom's policy requires employees to work in the office for a minimum of three days a week, unless additional in-office days are directed by their agency or manager. Our objective is to increase this requirement over time, and many of our agencies as well as Omnicom's corporate group already require five days of in-office attendance.
Omnicom is committed to hiring and developing exceptional talent. We agree that talent is uniquely distributed, and we're focused on developing inclusive teams that can bring the best solutions to everything we do. We strongly believe that celebrating what makes us different makes us better together. Join us-we look forward to getting to know you. We will process your personal data in accordance with our Recruitment Privacy Notice.
Link to Recruitment Privacy Notice: https://www.omc.com/privacy-notice
For US Job Seekers:
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Telecommunications
1 - 10 Employees
Glendale, CA, US