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Manager Adverse Event Reporting Jobs (NOW HIRING)

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 ...

Adverse Event Specialist

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 ...

Adverse Event Specialist

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 ...

Adverse Event Specialist

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 ...

Adverse Event Specialist

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 ...

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 ...

Adverse Event Specialist

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 ...

Senior Safety Specialist

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 ...

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Manager Adverse Event Reporting information

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How much do manager adverse event reporting jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for manager 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 is a manager adverse event reporting?

Manager Adverse Event Reporting jobs involve overseeing the process of identifying, documenting, and reporting adverse events related to pharmaceutical products, medical devices, or clinical trials. These managers ensure compliance with regulatory requirements, coordinate with cross-functional teams, and implement procedures to accurately capture and report safety data. They play a critical role in maintaining patient safety and regulatory compliance, often interacting with regulatory agencies and internal stakeholders. Strong knowledge of pharmacovigilance, regulatory guidelines, and project management is essential for this role.

What are some of the main challenges faced by a manager adverse event reporting, and how can they be addressed?

A Manager Adverse Event Reporting often faces challenges such as ensuring timely and accurate reporting of adverse events to regulatory authorities, managing large volumes of data, and staying updated with evolving regulatory requirements. Effective communication and collaboration with cross-functional teams like clinical, regulatory, and safety are essential to maintain compliance and data integrity. Utilizing robust pharmacovigilance systems and fostering ongoing training for team members can significantly mitigate these challenges and ensure smooth operations.

What are the key skills and qualifications needed to thrive as a manager adverse event reporting, and why are they important?

To thrive as a Manager Adverse Event Reporting, you need a strong background in pharmacovigilance, regulatory compliance, and life sciences, often supported by a relevant bachelor’s or advanced degree. Familiarity with safety databases, MedDRA coding, and global regulatory reporting systems such as EudraVigilance and FDA safety reporting tools is essential. Strong attention to detail, leadership, and excellent communication skills help ensure accurate reporting and effective team management. These competencies are crucial for maintaining patient safety, regulatory compliance, and the integrity of pharmacovigilance operations.
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The top searched job categories for Manager Adverse Event Reporting jobs are:

Infographic showing various Manager Adverse Event Reporting job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $53,254 per year, or $25.6 per hour.

Adverse Event Reporting Officer

Omnicom

Remote

$17 - $21.50/hr

Full-time

Re-posted 4 days ago


Job description

Agency:

Snow

Job Function:

General Legal

Job Subfunction:

Compliance and Regulatory


Job Description:

JOB SUMMARY:
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 transferrable skills for this position are problem solving, professionalism, compassion, communication, organization, the ability to work with minimal supervision, attention to detail, and resourcefulness.
Snow's business is centered around the patient journey, and the AERO, like all positions at Snow, must be open, compassionate, and sensitive to the unique life experiences of these patients and caregivers. The AERO must be able to incorporate the unique patient/caregiver experience into the strategies and solutions we provide to our clients.
ESSENTIAL JOB FUNCTIONS AND RESPONSBILITIES:
To perform this job successfully, the AERO must be able to perform each essential duty within the established guidelines. The requirements listed below are representative of the knowledge, skill, and/or ability required.
Prepare and submit product safety event forms in compliance with Snow standards and individual client requirements
Verify the accuracy and completeness of information for each adverse event report in conjunction with the source documents and ensure that the activities are performed in a manner consistent with company SOPs.
Interact cross functionally to confirm details and request additional information
Perform Source Data Verification (SDV) per Snow policies
Maintain working knowledge of FDA guidelines for adverse event/special events/product complaints
Perform retrospective quality review and document findings, and contribute to metric compilation
Assist with technical change processes and conduct quality reviews
Assist with risk analysis and corrective actions as identified in internal review of Salesforce and other documentation.
Suggest improvements, resolve problems, and recommend changes to procedures that will enhance Snow adherence to client and internal processes
Recommend changes that will improve quality, efficiency, and reduce cost
The primary job functions and responsibilities include, but are not limited to, those listed
Weekend & Night Work:
Snow Companies must report adverse events within 24 hours. Although day-to-day work should take place mostly during regular office hours (8:30 a.m.-6:00 p.m., Monday-Friday), candidates selected for the AERO position should have the expectation that the workload and nature of the work will require hours that extend past the business hours of the company. This includes working in the evening, on the weekends and required rotating Saturday hours.
Flexibility:
The core business hours that you work may change based on business needs and shifts may change from time to time.
Collaboration/Teamwork:
The expanding size and nature of our company will require that you work in collaboration with people in other departments. Candidates must demonstrate their willingness/ability to step into other roles as needed to drive the success of the company. Candidates will need to demonstrate their ability to be a contributing member of a team that has goals that are broader than an individual job description or function.
Language Skills/Communication:
Candidates must have the ability to read and comprehend general documents relating to the pharmaceutical/bio-technology industry that include, but are not limited to: medical education, medical periodicals, clinical trial data, package inserts, medical procedures and industry regulations for product safety event reporting and documentations. Candidates will have demonstrated their ability to effectively and professionally communicate with managers, clients, customers, mentors, and the general public. Working with patients requires the candidates to exercise discretion and empathy as patients are living with chronic conditions. Fluency in a foreign language is a plus, but not required.
Organization:
Candidates must have demonstrable organizational skills and can give clear examples of their ability to multitask and set priorities in a high-pressure environment. The importance of privacy means that recordkeeping, file management and version control are crucial.
Resourcefulness:
Product safety event reporting and internal quality assurance monitoring and auditing inherently requires a person to think quickly, have strong attention to detail, and be able to troubleshoot effectively. A demonstrated ability to anticipate hurdles, overcome them quickly and efficiently, and document the outcome and process changes needed is paramount. Team members are required to have a good understanding of patient privacy laws (HIPAA) as well as disease knowledge and sensitivity.
Patient Privacy:
The core of our business is working with patients. It is most likely that you will come in contact with Personal Consumer Information (PCI) of patients living with chronic illness. It will be required that you take training courses that include, but are not limited to:
Snow Policy Training
Health Insurance Portability and Accountability Act (HIPAA)
Adverse Event (AE) Reporting Training
US Food and Drug Administration (FDA) Training
Computer Skills:
Candidate must have excellent computer skills in a Microsoft Windows environment to include:
Word processors (Word)
Spreadsheets (Excel)
Presentation software (PowerPoint)
Email (Outlook)
Internet and World Wide Web
Salesforce (preferred)
Mathematical Skills:
Candidate will have the ability to comprehend and utilize basic mathematics as well as business statistics to include percentages, ratios, discounts, interest, commissions, and proportions.
Reasoning Ability:
Candidate will have the ability to identify and define problems while applying effective problem-solving skills through collecting data, establishing facts, and drawing valid conclusions. Candidate will have the ability to deal with a variety of concrete variables in situations where only limited standardization exists. Candidate will have the ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form. Candidate will be capable of applying industry benchmarks to create standardized practices.
Physical Demands:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand; walk; sit; use hands (to finger, handle, or feel); reach with hands and arms; and talk or hear. The employee must regularly lift and/or move up to 25 pounds and occasionally lift and/or move more than 25 pounds. Specific vision abilities required by this job include close vision, color vision, and ability to adjust focus.
Work Environment/Environmental Conditions:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually moderate. No or very limited exposure to physical risk.
Certificates, Licenses & Registrations:
Candidates must have a valid driver's license. In some instances, a passport may be necessary.
Education and Experience:
Bachelor's degree (B.A.) from a four-year college or university and/or one to two years of related experience and/or training preferred. Medical background preferred. Basic computer skills, including database data entry, and previous experience with patient communication a must.

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.