Adverse Event Reporting Officer
$17 - $21.50/hr
The importance of privacy means that recordkeeping, file management and version control are crucial ... Adverse Event (AE) Reporting Training US Food and Drug Administration (FDA) Training Computer ...
$17 - $21.50/hr
The importance of privacy means that recordkeeping, file management and version control are crucial ... Adverse Event (AE) Reporting Training US Food and Drug Administration (FDA) Training Computer ...
$17 - $21.50/hr
The importance of privacy means that recordkeeping, file management and version control are crucial ... Adverse Event (AE) Reporting Training US Food and Drug Administration (FDA) Training Computer ...
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize ... Tracking and reporting progress of specific Quality System indicators for management review;
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize ... Tracking and reporting progress of specific Quality System indicators for management review;
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize ... Tracking and reporting progress of specific Quality System indicators for management review;
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize ... Tracking and reporting progress of specific Quality System indicators for management review;
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize ... Tracking and reporting progress of specific Quality System indicators for management review;
The Adverse Event Reporting Team is responsible with implementation of best practices to optimize ... Tracking and reporting progress of specific Quality System indicators for management review;
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 ...
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 ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
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 ...
Niles, IL · On-site
$120 - $180/hr
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
$120 - $180/hr
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 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 ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. Proficiency with ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. Proficiency with ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
Mundelein, IL · On-site
$67K - $101K/yr
It ensures that all MDR submissions are completed in full compliance with FDA reporting ... Ability to manage multiple priorities and meet strict remediation timelines. * Proficiency with ...
Smyrna, GA · On-site
$64.75 - $76.25/hr
Lead medication safety, adverse event reporting, product complaint management, and pharmacovigilance activities. * Conduct investigations, root cause analyses, deviation reporting, and CAPA ...
Smyrna, GA · On-site
$64.75 - $76.25/hr
Lead medication safety, adverse event reporting, product complaint management, and pharmacovigilance activities. * Conduct investigations, root cause analyses, deviation reporting, and CAPA ...
Saint Petersburg, FL · On-site
$60 - $70.75/hr
Lead medication safety, adverse event reporting, product complaint management, and pharmacovigilance activities. * Conduct investigations, root cause analyses, deviation reporting, and CAPA ...
Saint Petersburg, FL · On-site
$60 - $70.75/hr
Lead medication safety, adverse event reporting, product complaint management, and pharmacovigilance activities. * Conduct investigations, root cause analyses, deviation reporting, and CAPA ...
NC · Remote
$75K - $126K/yr
Work independently to receive, triage, manage, and reconcile adverse event reports, including those reported in scientific literature, in accordance with contractual and regulatory timelines. Collect ...
New
NC · Remote
$75K - $126K/yr
Work independently to receive, triage, manage, and reconcile adverse event reports, including those reported in scientific literature, in accordance with contractual and regulatory timelines. Collect ...
New
Smyrna, GA · On-site
$64.75 - $76.25/hr
Lead medication safety, adverse event reporting, product complaint management, and pharmacovigilance activities. * Conduct investigations, root cause analyses, deviation reporting, and CAPA ...
Smyrna, GA · On-site
$64.75 - $76.25/hr
Lead medication safety, adverse event reporting, product complaint management, and pharmacovigilance activities. * Conduct investigations, root cause analyses, deviation reporting, and CAPA ...
$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
Cities with the most Manager Adverse Event Reporting job openings:
The most popular types of Adverse Event Reporting jobs are:
States with the most job openings for Manager Adverse Event Reporting jobs include:
The top searched job categories for Manager Adverse Event Reporting jobs are:

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:
It is the policy of Omnicom and any of its affiliates to provide equal employment opportunities to all employees and applicants for employment without regard to race, religion, color, ethnic origin, gender, gender identity, age, marital status, veteran status, sexual orientation, disability, or any other basis prohibited by applicable federal, state, or local law. EOE/AA/M/D/V/F.
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Telecommunications
1 - 10 Employees
Glendale, CA, US