... adverse event reporting process. 3. Analyzes and makes recommendations regarding complaints received by Merit to determine if they are reportable to global regulatory bodies. 4. Participates in ...
New
... adverse event reporting process. 3. Analyzes and makes recommendations regarding complaints received by Merit to determine if they are reportable to global regulatory bodies. 4. Participates in ...
New
Initiates, owns, or assists with internal audit and CAPA actions as they relate to complaint records and/or adverse event reporting * Participates in complaint record remediation planning and ...
Initiates, owns, or assists with internal audit and CAPA actions as they relate to complaint records and/or adverse event reporting * Participates in complaint record remediation planning and ...
Remote Summary: Responsible for timely preparation and submission of organized, scientifically ... Supports serious adverse event reporting, and completion of post-market surveillance activities ...
New
Remote Summary: Responsible for timely preparation and submission of organized, scientifically ... Supports serious adverse event reporting, and completion of post-market surveillance activities ...
New
This fully remote position is responsible for the development, implementation, coordination, and ... education, adverse-event reporting, and collaboration across neurology, radiology, infusion ...
New
This fully remote position is responsible for the development, implementation, coordination, and ... education, adverse-event reporting, and collaboration across neurology, radiology, infusion ...
New
This fully remote position is responsible for the development, implementation, coordination, and ... education, adverse-event reporting, and collaboration across neurology, radiology, infusion ...
New
This fully remote position is responsible for the development, implementation, coordination, and ... education, adverse-event reporting, and collaboration across neurology, radiology, infusion ...
New
Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies. * Performing case ...
Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies. * Performing case ...
Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies. * Performing case ...
Leading the collection, evaluation, and processing of adverse event reports to ensure timely and accurate reporting in accordance with regulatory guidelines and company policies. * Performing case ...
Project Manager, Regulatory Affairs
Irvine, CA · Remote
$140K/yr
Remote Summary: Responsible for timely preparation and submission of organized, scientifically ... Supports serious adverse event reporting, and completion of post-market surveillance activities ...
Project Manager, Regulatory Affairs
Irvine, CA · Remote
$140K/yr
Remote Summary: Responsible for timely preparation and submission of organized, scientifically ... Supports serious adverse event reporting, and completion of post-market surveillance activities ...
Clinical Navigator - Remote Patient Nutrition Support & Adherence, RN or Dietitian a Plus!
OR · Remote
This is a fully remote position. Preferred candidates possess telehealth/remote patient support ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
Clinical Navigator - Remote Patient Nutrition Support & Adherence, RN or Dietitian a Plus!
OR · Remote
This is a fully remote position. Preferred candidates possess telehealth/remote patient support ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
Clinical Navigator - Remote Patient Support, License Required, Oncology/Infusion a Plus!
Huntington Beach, CA · Remote
This is a fully remote position. Preferred candidates are able to work in Mountain or Pacific Time ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
Quick apply
Clinical Navigator - Remote Patient Support, License Required, Oncology/Infusion a Plus!
Huntington Beach, CA · Remote
This is a fully remote position. Preferred candidates are able to work in Mountain or Pacific Time ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
This is a fully remote position. Preferred candidates possess telehealth/remote patient support ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
This is a fully remote position. Preferred candidates possess telehealth/remote patient support ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
This is a fully remote position. Preferred candidates are able to work in Mountain or Pacific Time ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
This is a fully remote position. Preferred candidates are able to work in Mountain or Pacific Time ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
This is a fully remote position. Preferred candidates are able to work in Mountain or Pacific Time ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
This is a fully remote position. Preferred candidates are able to work in Mountain or Pacific Time ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
Clinical Navigator - Remote Patient Nutrition Support & Adherence, RN or Dietitian a Plus!
Huntington Beach, CA · Remote
This is a fully remote position. Preferred candidates possess telehealth/remote patient support ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
Quick apply
Clinical Navigator - Remote Patient Nutrition Support & Adherence, RN or Dietitian a Plus!
Huntington Beach, CA · Remote
This is a fully remote position. Preferred candidates possess telehealth/remote patient support ... Identify and report adverse events, product complaints, medication errors, missed or delayed ...
Medical Information Specialist
Overland Park, KS · On-site +1
Knowledge of FDA's postmarketing adverse event reporting regulations and safety terminology. Ability to make accurate assessments regarding what information needs to be obtained and level or depth of ...
Medical Information Specialist
Overland Park, KS · On-site +1
Knowledge of FDA's postmarketing adverse event reporting regulations and safety terminology. Ability to make accurate assessments regarding what information needs to be obtained and level or depth of ...
Workflow Manager, Pharmacovigilance Operations (Specialist II, PSS) Remote based (US or Canada)
Durham, NC · Remote
Manage the receipt and processing of all adverse event reports reported either spontaneously from ... Work Environment: * Work is performed in a remote based office environment with exposure to ...
Workflow Manager, Pharmacovigilance Operations (Specialist II, PSS) Remote based (US or Canada)
Durham, NC · Remote
Manage the receipt and processing of all adverse event reports reported either spontaneously from ... Work Environment: * Work is performed in a remote based office environment with exposure to ...
Knowledge of FDA's postmarketing adverse event reporting regulations and safety terminology. Ability to make accurate assessments regarding what information needs to be obtained and level or depth of ...
Knowledge of FDA's postmarketing adverse event reporting regulations and safety terminology. Ability to make accurate assessments regarding what information needs to be obtained and level or depth of ...
Previous experience with adverse event reporting systems, FDA and EU drug safety/Pharmacovigilance ... remote position with employees working from a home office. The physical demands described are ...
Previous experience with adverse event reporting systems, FDA and EU drug safety/Pharmacovigilance ... remote position with employees working from a home office. The physical demands described are ...
Clinicia Expert - Remote
San Jose, CA · Remote
$150 - $200/hr
Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution ... reports, safety narratives, and DSMB/IDMC materials. * Strong understanding of oncology and ...
New
Quick apply
Clinicia Expert - Remote
San Jose, CA · Remote
$150 - $200/hr
Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution ... reports, safety narratives, and DSMB/IDMC materials. * Strong understanding of oncology and ...
New
Clinicia Expert - Remote
Seattle, WA · Remote
$150 - $200/hr
Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution ... reports, safety narratives, and DSMB/IDMC materials. * Strong understanding of oncology and ...
New
Quick apply
Clinicia Expert - Remote
Seattle, WA · Remote
$150 - $200/hr
Assess dose escalation strategies, dose-limiting toxicities, adverse event grading, attribution ... reports, safety narratives, and DSMB/IDMC materials. * Strong understanding of oncology and ...
New
Adverse Event Reporting Remote information
See salary details
$12.26 - $18.95
7% of jobs
$18.95 - $25.63
4% of jobs
$25.63 - $32.32
3% of jobs
$38.25 is the 25th percentile. Wages below this are outliers.
$32.32 - $39.01
12% of jobs
The median wage is $44.20 / hr.
$39.01 - $45.69
31% of jobs
$45.69 - $52.38
15% of jobs
$54.36 is the 75th percentile. Wages above this are outliers.
$52.38 - $59.07
12% of jobs
$59.07 - $65.76
0% of jobs
$65.76 - $72.44
9% of jobs
$72.44 - $79.13
5% of jobs
$79.13 - $85.82
2% of jobs
$12
$49
$85
How much do adverse event reporting remote jobs pay per hour?
As of Aug 14, 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 the difference between Adverse Event Reporting Remote vs Clinical Data Coordinator?
| Aspect | Adverse Event Reporting Remote | Clinical Data Coordinator |
|---|---|---|
| Required credentials | Life sciences degree, certification in pharmacovigilance preferred | Healthcare or life sciences degree, data management certifications |
| Work environment | Remote, primarily computer-based, often independent | Office or remote, involves data entry and management |
| Employer and industry usage | Pharmaceutical companies, CROs, biotech firms | Hospitals, research institutions, pharma companies |
| Common search and comparison intent | Understanding remote pharmacovigilance roles | Managing 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.
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 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 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.
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:
What job categories do people searching Adverse Event Reporting Remote jobs look for?
The top searched job categories for Adverse Event Reporting Remote jobs are:
Full-time
Medical, Retirement, PTO
Posted 3 days ago
New
Merit Medical Systems rating
7.0
Based on 18 frontline employees who took The Breakroom Quiz
Job description
Work Shift:
DAY
Work Schedule:
Why Merit?
At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.
This position is a fixed-term opportunity currently expected to run through March 2027.
ESSENTIAL FUNCTIONS PERFORMED
1. Maintains and implements improvement projects and provides training when needed.
2. Interacts with various levels of management, international regulatory affairs/quality assurance, and global regulatory bodies on the adverse event reporting process.
3. Analyzes and makes recommendations regarding complaints received by Merit to determine if they are reportable to global regulatory bodies.
4. Participates in complaint related meetings to determine which complaints require an adverse event report.
5. Reviews complaint investigations and makes recommendations for resolution.
6. Prepares and submits necessary reports to global regulatory bodies within the required timeframe for each agency and report type.
7. Maintains appropriate records for the Global Quality Assurance adverse event reporting system as defined in relevant procedures.
8. Prepares for, participates in and assists with FDA facility inspections, Notified Body Audits, Post Market Surveillance activities and other governmental inspections as directed.
9. Performs other duties and tasks, as needed.
ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS
• Lifting -- Not to exceed 50 lbs. - local practice may apply.
• Writing
• Sitting
• Standing
• Bending
• Visual acuity
• Color perception
• Depth perception
• Reading
• Field of vision/peripheral
SUMMARY OF MINIMUM QUALIFICATIONS
• Education and/or experience equivalent to a Bachelor's Degree and three years of related experience in a Quality/Regulatory related field.
• Knowledge of U.S. FDA regulations (21 CFR 803), the Medical Devices Directive (93/42/EEC, as amended), the European Medical Device Regulation 2017/745 (MDR), ISO 13485 Quality System Standards, and Canadian Medical Device Regulations.
• Experience with medical device global adverse event reporting required, such as MDR, MPR, and Vigilance, TGA, etc.
• Self-motivated, self-directing, strong attention to detail and excellent time management skills.
• Strong interpersonal skills and the ability to communicate well - verbally and in writing - with others.
• Project management experience.
• Demonstrated computer skills preferably spreadsheets, word processing, database, internet research and other applicable software programs.
PREFERRED QUALIFICATIONS
• American Society for Quality (ASQ) Certifications - Certified Quality Auditor (CQA)
• Regulatory Affairs Certification - RAC (Global).
• Experience with electronic submissions.
COMPETENCIES
• Global medical device adverse event reporting, such as MDR, MPR, TGA, and Vigilance
• Computer skills/internet research
• Interpersonal/communication skills
• Quality system development/training
COMMENTS
Infectious Control Risk Category II:
The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category II states employment and procedures that may require exposure.
As an eligible Merit employee, you can expect the following:
* Multiple Shifts and Hours to choose from: Days, Swing (Eve), and Nights
* Medical/Dental & Other Insurances (eligible the first of month after 30 days)
* Low Cost Onsite Medical Clinic
* Two (2) Onsite Cafeterias
* Employee Garden | Gardening Classes
* 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays
* 401K | Health Savings Account
To see more on our culture, go to www.merit.com/careers.
Military Veterans are encouraged to Apply.
Merit is a proud Utah Patriot Partner committed to hiring our Veterans.
DAY
Work Schedule:
Why Merit?
At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.
This position is a fixed-term opportunity currently expected to run through March 2027.
ESSENTIAL FUNCTIONS PERFORMED
1. Maintains and implements improvement projects and provides training when needed.
2. Interacts with various levels of management, international regulatory affairs/quality assurance, and global regulatory bodies on the adverse event reporting process.
3. Analyzes and makes recommendations regarding complaints received by Merit to determine if they are reportable to global regulatory bodies.
4. Participates in complaint related meetings to determine which complaints require an adverse event report.
5. Reviews complaint investigations and makes recommendations for resolution.
6. Prepares and submits necessary reports to global regulatory bodies within the required timeframe for each agency and report type.
7. Maintains appropriate records for the Global Quality Assurance adverse event reporting system as defined in relevant procedures.
8. Prepares for, participates in and assists with FDA facility inspections, Notified Body Audits, Post Market Surveillance activities and other governmental inspections as directed.
9. Performs other duties and tasks, as needed.
ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS
• Lifting -- Not to exceed 50 lbs. - local practice may apply.
• Writing
• Sitting
• Standing
• Bending
• Visual acuity
• Color perception
• Depth perception
• Reading
• Field of vision/peripheral
SUMMARY OF MINIMUM QUALIFICATIONS
• Education and/or experience equivalent to a Bachelor's Degree and three years of related experience in a Quality/Regulatory related field.
• Knowledge of U.S. FDA regulations (21 CFR 803), the Medical Devices Directive (93/42/EEC, as amended), the European Medical Device Regulation 2017/745 (MDR), ISO 13485 Quality System Standards, and Canadian Medical Device Regulations.
• Experience with medical device global adverse event reporting required, such as MDR, MPR, and Vigilance, TGA, etc.
• Self-motivated, self-directing, strong attention to detail and excellent time management skills.
• Strong interpersonal skills and the ability to communicate well - verbally and in writing - with others.
• Project management experience.
• Demonstrated computer skills preferably spreadsheets, word processing, database, internet research and other applicable software programs.
PREFERRED QUALIFICATIONS
• American Society for Quality (ASQ) Certifications - Certified Quality Auditor (CQA)
• Regulatory Affairs Certification - RAC (Global).
• Experience with electronic submissions.
COMPETENCIES
• Global medical device adverse event reporting, such as MDR, MPR, TGA, and Vigilance
• Computer skills/internet research
• Interpersonal/communication skills
• Quality system development/training
COMMENTS
Infectious Control Risk Category II:
The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs. Risk category II states employment and procedures that may require exposure.
As an eligible Merit employee, you can expect the following:
* Multiple Shifts and Hours to choose from: Days, Swing (Eve), and Nights
* Medical/Dental & Other Insurances (eligible the first of month after 30 days)
* Low Cost Onsite Medical Clinic
* Two (2) Onsite Cafeterias
* Employee Garden | Gardening Classes
* 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays
* 401K | Health Savings Account
To see more on our culture, go to www.merit.com/careers.
Military Veterans are encouraged to Apply.
Merit is a proud Utah Patriot Partner committed to hiring our Veterans.
What Merit Medical Systems employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Merit Medical Systems
Sourced by ZipRecruiter
Industry
Medical equipment and supplies manufacturing
Company size
5,001 - 10,000 Employees
Headquarters location
South Jordan, UT, US
Year founded
1987