Los Angeles, CA 90032 Duration- 4 months (Possible extension for long term) FAQ This position is for Adverse event monitoring. This person will deal with marketed products and side effects, follow up ...
Quick apply
Los Angeles, CA 90032 Duration- 4 months (Possible extension for long term) FAQ This position is for Adverse event monitoring. This person will deal with marketed products and side effects, follow up ...
This role provides scientific support to FDA efforts around cosmetic product registration, listing, ingredient safety assessment, adverse event analysis, and the development of tools, guidance, and ...
This role provides scientific support to FDA efforts around cosmetic product registration, listing, ingredient safety assessment, adverse event analysis, and the development of tools, guidance, and ...
Qualifications - Provide initial medical evaluation of adverse events on company investigational and marketed products by determining the seriousness, expectedness, and therefore reportability of ...
Qualifications - Provide initial medical evaluation of adverse events on company investigational and marketed products by determining the seriousness, expectedness, and therefore reportability of ...
Medical Device Complaint Specialist
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
Medical Device Complaint Specialist
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 ...
Drug Safety Specialist
Waltham, MA · On-site
We are seeking a Drug Safety Specialist with 3-5 years of pharmacovigilance experience and a clinical background (RN, BSN, RPh, or PharmD) to support adverse event case processing for marketed and ...
Drug Safety Specialist
Waltham, MA · On-site
We are seeking a Drug Safety Specialist with 3-5 years of pharmacovigilance experience and a clinical background (RN, BSN, RPh, or PharmD) to support adverse event case processing for marketed and ...
Regulatory Specialist, Beauty & Wellness
Marlborough, MA · On-site
$70K - $88K/yr
Determine if and potential adverse events/adverse events require a field action or CAPA to be taken on any given product line. * Coordinate the adverse event reporting process required to the ...
Regulatory Specialist, Beauty & Wellness
Marlborough, MA · On-site
$70K - $88K/yr
Determine if and potential adverse events/adverse events require a field action or CAPA to be taken on any given product line. * Coordinate the adverse event reporting process required to the ...
Will be responsible for several portions of the adverse event case processing workflow including but not limited to receipt, evaluation, registration, partial data entry, documentation, and reporting ...
Will be responsible for several portions of the adverse event case processing workflow including but not limited to receipt, evaluation, registration, partial data entry, documentation, and reporting ...
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 ...
Medical Device Complaint Specialist
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
Medical Device Complaint Specialist
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 ...
Risk Management Analyst
San Francisco, CA · On-site
The Coordinator provides risk advice in a variety of areas, including consent, mandatory reporting, patient/family/visitor behavior, threat management, medication management, adverse event management ...
Risk Management Analyst
San Francisco, CA · On-site
The Coordinator provides risk advice in a variety of areas, including consent, mandatory reporting, patient/family/visitor behavior, threat management, medication management, adverse event management ...
Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate adverse event and product complaint reports in compliance with EVERSANA-MICC ...
Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate adverse event and product complaint reports in compliance with EVERSANA-MICC ...
Quality Assurance Post Market Specialist
Redmond, WA · On-site
$83K - $139K/yr
Review product complaints and adverse event reports to assess reportability and determine whether device use contributed to patient harm. * Interface with customers to collect patient information and ...
Quality Assurance Post Market Specialist
Redmond, WA · On-site
$83K - $139K/yr
Review product complaints and adverse event reports to assess reportability and determine whether device use contributed to patient harm. * Interface with customers to collect patient information and ...
This role involves reviewing and evaluating serious adverse event reports (SAERs) and Adverse Events of Special Interest (AESI) to ensure compliance with regulatory reporting requirements ...
This role involves reviewing and evaluating serious adverse event reports (SAERs) and Adverse Events of Special Interest (AESI) to ensure compliance with regulatory reporting requirements ...
This role involves reviewing and evaluating serious adverse event reports (SAERs) and Adverse Events of Special Interest (AESI) to ensure compliance with regulatory reporting requirements ...
This role involves reviewing and evaluating serious adverse event reports (SAERs) and Adverse Events of Special Interest (AESI) to ensure compliance with regulatory reporting requirements ...
Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate adverse event and product complaint reports in compliance with EVERSANA-MICC ...
Quick apply
Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate adverse event and product complaint reports in compliance with EVERSANA-MICC ...
Responds to all sentinel/serious adverse events and conducts a thorough case review and chronology. In conjunction with leadership team, determines whether an event review/root cause analysis session ...
Responds to all sentinel/serious adverse events and conducts a thorough case review and chronology. In conjunction with leadership team, determines whether an event review/root cause analysis session ...
Responds to all sentinel/serious adverse events and conducts a thorough case review and chronology. In conjunction with leadership team, determines whether an event review/root cause analysis session ...
Responds to all sentinel/serious adverse events and conducts a thorough case review and chronology. In conjunction with leadership team, determines whether an event review/root cause analysis session ...
Medical Information Specialist
Overland Park, KS · On-site +1
Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate adverse event and product complaint reports in compliance with EVERSANA-MICC ...
Medical Information Specialist
Overland Park, KS · On-site +1
Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate adverse event and product complaint reports in compliance with EVERSANA-MICC ...
Responds to all sentinel/serious adverse events and conducts a thorough case review and chronology. In conjunction with leadership team, determines whether an event review/root cause analysis session ...
Responds to all sentinel/serious adverse events and conducts a thorough case review and chronology. In conjunction with leadership team, determines whether an event review/root cause analysis session ...
Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate adverse event and product complaint reports in compliance with EVERSANA-MICC ...
Identify adverse events and product complaints during interactions with customers. Perform intake sufficient to generate adverse event and product complaint reports in compliance with EVERSANA-MICC ...
Adverse Event 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 jobs pay per hour?
As of Aug 17, 2026, the average hourly pay for adverse event 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 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.
More about Adverse Event jobs
What states have the most Adverse Event jobs?
States with the most job openings for Adverse Event jobs include:
What job categories do people searching Adverse Event jobs look for?
The top searched job categories for Adverse Event jobs are:
Job description
Title: Pharmacovigilance Specialist
Location: Los Angeles, CA 90032
Duration- 4 months (Possible extension for long term)
FAQ
This position is for Adverse event monitoring. This person will deal with marketed products and side effects, follow up with reporters (patients, Doctors, etc.), and triage case reports. Looking for someone with a background in Pharmacovigilance who can follow international regulatory guidelines.
Preference is for the ARGUS database. PSUR exp would be nice.
The interview will consist of a phone screen with the local manager and a second phone screen with management in Barcelona. The team is based in LA, but it is a global team and will need someone who can be flexible in scheduling meetings across multiple time zones.
Summary:
- Provides operational support for global pharmacovigilance activities of client's marketed products.
- Ensures pharmacovigilance deliverables are of the highest quality and meet global regulatory reporting timelines.
- Responsible for data review, compilation, and analysis, including management of the integrated safety database.
- Management of Adverse Events including activities such as processing adverse event case reports and conducts follow-up .
- Notifies regulatory agencies and business partners accordingly; responds to requests from regulatory agencies
- Reviews scientific literature and bibliographic sources; draft and manage periodic safety update reports. .
- Evaluates safety profiles; draft and manage signal detection reports; ensures document filing and archiving. .
- Participation in the processes involving the collection, processing, review and distribution of adverse event information regarding development and marketed client's pharmaceutical products. .
- Contributes to ensure compliance of pharmacovigilance activities including activities such as conduct case reconciliation with concerned departments, affiliates, distributors or business partners .
- Take part in self-inspection visits, audits, inspections and in CAPAs management, create or update pharmacovigilance procedures and working practices .
- Provide training to concerned persons based on the training plan and managing training documentation; archive documents according to prevailing standards .
- Support in the procedures of global pharmacovigilance operations such as Standard Operation Procedures (SOPs), internal business practices or working instructions. .
- Serves in an advisory capacity including activities such as product monographs review, draft responses to pharmacovigilance requests from regulatory agencies; participates in the drafting and implementation of pharmacovigilance contracts and agreements. be sure to see notes before submitting candidates.
Questions to be answered
- List specific areas of expertise in Pharmacovigilance you have focused on.
- What safety database(s) have you used, and what types of cases have you processed?
About Rishabh BPO Services
Sourced by ZipRecruiter
Rishabh BPO is the right choice for companies looking to outsource their business processes to lower their costs, eventually resulting in a transformation of the way the company works. The general benefits of BPO are well known in the industry today. Long term approach of engaging with the customers: This means that Rishabh BPO will focus on getting value for their customers by investing their own resources in the short-term so that the clients experience the value of working with Rishabh BPO over the entire engagement.
Industry
Business management consulting
Company size
51 - 200 Employees
Headquarters location
San Jose, CA, US