Also engages in adverse event reporting , product quality complaint reporting, and other processes as required. * Completes special assignments. Interacts with business partners external to the MIC.
Also engages in adverse event reporting , product quality complaint reporting, and other processes as required. * Completes special assignments. Interacts with business partners external to the MIC.
Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB activities and safety reviews * Develop and manage clinical ...
Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB activities and safety reviews * Develop and manage clinical ...
S. adverse event reports is critical for the company to maintain compliance with local and international regulations. Additional responsibilities include data management activities associated with ...
S. adverse event reports is critical for the company to maintain compliance with local and international regulations. Additional responsibilities include data management activities associated with ...
Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB activities and safety reviews * Develop and manage clinical ...
Quick apply
Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB activities and safety reviews * Develop and manage clinical ...
Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB activities and safety reviews * Develop and manage clinical ...
Oversee adverse event reporting and pharmacovigilance systems * Ensure compliance with GCP and regulatory requirements * Coordinate DSMB activities and safety reviews * Develop and manage clinical ...
S. adverse event reports is critical for the company to maintain compliance with local and international regulations. Additional responsibilities include data management activities associated with ...
S. adverse event reports is critical for the company to maintain compliance with local and international regulations. Additional responsibilities include data management activities associated with ...
Perform intake & generate accurate adverse event and product complaint reports in compliance with EVERSANA-MICC and client standard operating procedures. * Demonstrate knowledge of FDA's post ...
Perform intake & generate accurate adverse event and product complaint reports in compliance with EVERSANA-MICC and client standard operating procedures. * Demonstrate knowledge of FDA's post ...
Hospital Inpatient Pharmacist (Nightshift)
Tucson, AZ · On-site
$2.4K - $2.4K/wk
Monitor drug safety, interactions, and adverse event reporting. * Ensure compliance with regulatory standards and internal policies. * Participate in daily/nightly rounds with physicians and nursing ...
Quick apply
Hospital Inpatient Pharmacist (Nightshift)
Tucson, AZ · On-site
$2.4K - $2.4K/wk
Monitor drug safety, interactions, and adverse event reporting. * Ensure compliance with regulatory standards and internal policies. * Participate in daily/nightly rounds with physicians and nursing ...
Adverse event reporting and monitoring * Tort claim processing * Death and disability case reviews * Administrative and clinical adverse actions Policy & Documentation * Draft headquarters-level ...
Adverse event reporting and monitoring * Tort claim processing * Death and disability case reviews * Administrative and clinical adverse actions Policy & Documentation * Draft headquarters-level ...
Risk Manager-Hospital
Pomona, CA · On-site
$150K - $180K/yr
California Department of Public Health adverse event reporting requirements * Partner with leadership and department managers to implement risk-reduction strategies and improve operational processes.
Risk Manager-Hospital
Pomona, CA · On-site
$150K - $180K/yr
California Department of Public Health adverse event reporting requirements * Partner with leadership and department managers to implement risk-reduction strategies and improve operational processes.
Adverse event reporting and monitoring * Tort claim processing * Death and disability case reviews * Administrative and clinical adverse actions Policy & Documentation * Draft headquarters-level ...
Adverse event reporting and monitoring * Tort claim processing * Death and disability case reviews * Administrative and clinical adverse actions Policy & Documentation * Draft headquarters-level ...
Ensure adverse event reports (i.e. MDRs, ICSRs) are processed, prepared, and submitted to the FDA within regulation timelines. * Process FDA reportable post-market complaints and assist in ...
Ensure adverse event reports (i.e. MDRs, ICSRs) are processed, prepared, and submitted to the FDA within regulation timelines. * Process FDA reportable post-market complaints and assist in ...
Manage clinical trial operations from startup through closeout Oversee adverse event reporting and pharmacovigilance systems Ensure compliance with ICH-GCP and regulatory requirements Coordinate DSMB ...
Manage clinical trial operations from startup through closeout Oversee adverse event reporting and pharmacovigilance systems Ensure compliance with ICH-GCP and regulatory requirements Coordinate DSMB ...
Adverse event reporting and monitoring * Tort claim processing * Death and disability case reviews * Administrative and clinical adverse actions Policy & Documentation * Draft headquarters-level ...
Adverse event reporting and monitoring * Tort claim processing * Death and disability case reviews * Administrative and clinical adverse actions Policy & Documentation * Draft headquarters-level ...
Requirements Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH ...
Requirements Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH ...
Ensure adverse event reports (i.e. MDRs, ICSRs) are processed, prepared, and submitted to the FDA within regulation timelines. * Process FDA reportable post-market complaints and assist in ...
Ensure adverse event reports (i.e. MDRs, ICSRs) are processed, prepared, and submitted to the FDA within regulation timelines. * Process FDA reportable post-market complaints and assist in ...
Clinical Research Assistant
Santa Barbara, CA · On-site
$20.50 - $25/hr
Promptly request all necessary medical records for Serious Adverse Event Reporting * Process and ship laboratory biological samples for analysis * Perform intraocular pressure checks after injections
Clinical Research Assistant
Santa Barbara, CA · On-site
$20.50 - $25/hr
Promptly request all necessary medical records for Serious Adverse Event Reporting * Process and ship laboratory biological samples for analysis * Perform intraocular pressure checks after injections
Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and ...
Quick apply
Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and ...
Ensure adverse event reports (i.e. MDRs, ICSRs) are processed, prepared, and submitted to the FDA within regulation timelines. * Process FDA reportable post-market complaints and assist in ...
Ensure adverse event reports (i.e. MDRs, ICSRs) are processed, prepared, and submitted to the FDA within regulation timelines. * Process FDA reportable post-market complaints and assist in ...
Clinical Research Assistant
Oxnard, CA · On-site
$20.50 - $25/hr
Promptly request all necessary medical records for Serious Adverse Event Reporting * Process and ship laboratory biological samples for analysis * Perform intraocular pressure checks after injections
Clinical Research Assistant
Oxnard, CA · On-site
$20.50 - $25/hr
Promptly request all necessary medical records for Serious Adverse Event Reporting * Process and ship laboratory biological samples for analysis * Perform intraocular pressure checks after injections
Adverse Event Reporting information
See salary details
$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
How much do adverse event reporting jobs pay per hour?
As of Jul 14, 2026, the average hourly pay for adverse event reporting in the United States is $25.60, according to ZipRecruiter salary data. Most workers in this role earn between $22.36 and $28.61 per hour, depending on experience, location, and employer.
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 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 is an Adverse Event Reporting job?
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.
More about Adverse Event Reporting jobs
What cities are hiring for Adverse Event Reporting jobs? Cities with the most Adverse Event Reporting job openings:
What are the most commonly searched types of Adverse Event Reporting jobs? The most popular types of Adverse Event Reporting jobs are:
What states have the most Adverse Event Reporting jobs? States with the most job openings for Adverse Event Reporting jobs include:
What job categories do people searching Adverse Event Reporting jobs look for? The top searched job categories for Adverse Event Reporting jobs are:
- Clinical Research Relocation
- Clinical Trials Test Subject
- Research Coordinator
- Full Time Clinical Research Regulatory
- Clinical Research Organization
- Clinical Research Coordinator (Crc)
- Associate Research Coordinator
- Full Time Clinical Research Associate
- Seasonal Clinical Study Startup
- Clinical Research Coordinator 2
Full-time
Posted 27 days ago
Job description
Company Description
Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.
Job Description
- Serves as front line therapeutic specialist responsible for engaging healthcare professional customers in rich clinical dialogue and providing such customer support as clinical presentations, literature searches and other therapeutic activities as needed.
- Also engages in adverse event reporting, product quality complaint reporting, and other processes as required.
- Completes special assignments. Interacts with business partners external to the MIC.
- Collaborates with Medical Information on the development/updating of standard clinical replies.
- Provides timely, accurate, thorough and balanced responses to unsolicited requests for information from internal and external customers consistent with regulatory guidelines.
- Documents interactions in Department database.
- Identifies captures and processes adverse events and product quality complaints following Department procedures.
- Conducts literature analysis to respond to unsolicited, off-label inquiries as needed.
Additional Information
Kind Regards,
Sasha Sharma
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
DIRECT # - 732-662-7964
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996