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Adverse Event Reporting Remote Jobs (NOW HIRING)

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 ...

Senior Safety Specialist

NC · Remote

$75K - $126K/yr

Perform day-to-day adverse event reporting and subsequent Pharmacovigilance (PVG) activities performed within a highly regulated environment and driven by strict timelines. Work independently to ...

New

... and interpretation of adverse events and device deficiencies reported by clinical trial ... The Duties of this job can be performed remote or onsite. The physical demands described here are ...

... reports, adverse event reporting and complaints log and trend maintenance. Responsibilities ... Remote - US Actual compensation may vary depending on job-related factors including knowledge ...

Participates in adverse event reporting and safety responsibilities monitoring. * Coordinates and ... Remote ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 75 % of the Time MEDICAL ...

Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution ... reports, safety narratives, and DSMB/IDMC materials. * Strong understanding of oncology and ...

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Adverse Event Reporting Remote information

See salary details

$12

$49

$85

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

As of Sep 3, 2026, the average hourly pay for adverse event reporting remote in the United States is $49.14, according to ZipRecruiter salary data. Most workers in this role earn between $38.46 and $55.53 per hour, depending on experience, location, and employer.

What is adverse event reporting in a remote role?

Adverse event reporting in a remote role involves monitoring, documenting, and submitting reports about any negative or unintended effects experienced by patients during clinical trials or after using pharmaceutical products. Remote professionals in this field collect data from various sources, assess the severity and causality of the events, and ensure timely communication with regulatory authorities. The work is performed off-site using secure digital systems, requiring strong attention to detail, regulatory knowledge, and adherence to confidentiality protocols.

What are the key skills and qualifications needed to thrive in adverse event reporting remote, and why are they important?

To thrive in Adverse Event Reporting remotely, you need a solid understanding of pharmacovigilance principles, data analysis, and regulatory requirements, typically supported by a degree in life sciences or healthcare. Familiarity with safety databases like Argus or MedDRA coding, and experience using electronic reporting systems are essential. Attention to detail, strong written communication, and the ability to work independently are crucial soft skills for this role. These skills ensure accurate reporting, regulatory compliance, and timely identification of drug safety concerns, all of which protect patient health and company reputation.

What are some common challenges faced by professionals in remote adverse event reporting roles, and how can they be addressed?

Remote Adverse Event Reporting professionals often encounter challenges such as maintaining clear and timely communication with cross-functional teams, ensuring data accuracy without in-person supervision, and staying up-to-date with evolving regulatory requirements. To overcome these, it is important to establish strong communication routines, utilize secure digital platforms for collaborative documentation, and regularly participate in virtual training sessions. Being proactive about asking questions and seeking feedback can also help ensure compliance and high-quality reporting in a remote setting.

What is the difference between Adverse Event Reporting Remote vs Clinical Data Coordinator?

AspectAdverse Event Reporting RemoteClinical Data Coordinator
Required credentialsLife sciences degree, certification in pharmacovigilance preferredHealthcare or life sciences degree, data management certifications
Work environmentRemote, primarily computer-based, often independentOffice or remote, involves data entry and management
Employer and industry usagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, pharma companies
Common search and comparison intentUnderstanding remote pharmacovigilance rolesManaging clinical data in research settings

Adverse Event Reporting Remote focuses on monitoring and reporting drug safety incidents remotely, requiring pharmacovigilance knowledge. Clinical Data Coordinators manage clinical trial data, often in healthcare or research settings. While both roles involve data handling, Adverse Event Reporting Remote emphasizes safety reporting, whereas Clinical Data Coordinators focus on data accuracy and integrity in clinical studies.

More about Adverse Event Reporting Remote jobs

What cities are hiring for Adverse Event Reporting Remote jobs?

Cities with the most Adverse Event Reporting Remote 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 Remote jobs?

States with the most job openings for Adverse Event Reporting Remote jobs include:

Infographic showing various Adverse Event Reporting Remote job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 11% Part Time, 1% Temporary, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution, with an average salary of $102,217 per year, or $49.1 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.


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