Des Moines, IA · On-site +1
$56.75 - $68.25/hr
Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals. Qualifications: * PharmD with strong understanding of ...
Des Moines, IA · On-site +1
$56.75 - $68.25/hr
Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals. Qualifications: * PharmD with strong understanding of ...
Modesto, CA · On-site +1
$61.50 - $74/hr
Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals. Qualifications: * PharmD with strong understanding of ...
Modesto, CA · On-site +1
$61.50 - $74/hr
Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals. Qualifications: * PharmD with strong understanding of ...
Baton Rouge, LA · On-site +1
$56 - $67.25/hr
Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals. Qualifications: * PharmD with strong understanding of ...
Baton Rouge, LA · On-site +1
$56 - $67.25/hr
Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals. Qualifications: * PharmD with strong understanding of ...
Boise, ID · On-site +1
$50.50 - $60.50/hr
Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals. Qualifications: * PharmD with strong understanding of ...
Boise, ID · On-site +1
$50.50 - $60.50/hr
Prepare regulatory submissions (e.g., MedWatch, PSURs). * Collaborate with medical affairs and clinical teams to address safety signals. Qualifications: * PharmD with strong understanding of ...
Author Medical Device Reports (MDRs), MedWatch reports, vigilance reports and other regulatory submissions, ensuring timely transmission to appropriate regulatory authorities. Apply event coding to ...
Author Medical Device Reports (MDRs), MedWatch reports, vigilance reports and other regulatory submissions, ensuring timely transmission to appropriate regulatory authorities. Apply event coding to ...
$60K - $76K/yr
Knowledge of NABP license portals, MedWatch reporting, or REMS programs * Regulatory Affairs Certification (RAC) or DEA compliance training (preferred) * Experience responding to FDA inspections ...
$60K - $76K/yr
Knowledge of NABP license portals, MedWatch reporting, or REMS programs * Regulatory Affairs Certification (RAC) or DEA compliance training (preferred) * Experience responding to FDA inspections ...
Carlsbad, CA · On-site
... MedWatch reports, vigilance reports and other regulatory submissions, ensuring timely transmission to appropriate regulatory authorities. ● Apply event coding to support product performance records ...
Carlsbad, CA · On-site
... MedWatch reports, vigilance reports and other regulatory submissions, ensuring timely transmission to appropriate regulatory authorities. ● Apply event coding to support product performance records ...
Carlsbad, CA · On-site
... MedWatch reports, vigilance reports and other regulatory submissions, ensuring timely transmission to appropriate regulatory authorities. • Apply event coding to support product performance records ...
Carlsbad, CA · On-site
... MedWatch reports, vigilance reports and other regulatory submissions, ensuring timely transmission to appropriate regulatory authorities. • Apply event coding to support product performance records ...
Rockville, MD · Remote
Reviews the FDA MedWatch Alerts, safety communications and or other communications from other relevant Regulatory Authorities and recommends action for implementation by study teams, as applicable.
Rockville, MD · Remote
Reviews the FDA MedWatch Alerts, safety communications and or other communications from other relevant Regulatory Authorities and recommends action for implementation by study teams, as applicable.
Irvine, CA · On-site
$60K - $76K/yr
Knowledge of NABP license portals, MedWatch reporting, or REMS programs * Regulatory Affairs Certification (RAC) or DEA compliance training (preferred) * Experience responding to FDA inspections ...
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Irvine, CA · On-site
$60K - $76K/yr
Knowledge of NABP license portals, MedWatch reporting, or REMS programs * Regulatory Affairs Certification (RAC) or DEA compliance training (preferred) * Experience responding to FDA inspections ...
Irvine, CA · On-site
$60K - $76K/yr
Knowledge of NABP license portals, MedWatch reporting, or REMS programs * Regulatory Affairs Certification (RAC) or DEA compliance training (preferred) * Experience responding to FDA inspections ...
Irvine, CA · On-site
$60K - $76K/yr
Knowledge of NABP license portals, MedWatch reporting, or REMS programs * Regulatory Affairs Certification (RAC) or DEA compliance training (preferred) * Experience responding to FDA inspections ...
Minnetonka, MN · On-site
$30 - $32/hr
Draft Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring timely transmission to the appropriate regulatory authorities. * Apply codes to events to facilitate ...
Minnetonka, MN · On-site
$30 - $32/hr
Draft Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring timely transmission to the appropriate regulatory authorities. * Apply codes to events to facilitate ...
Lake Mary, FL · Remote
$62K - $74K/yr
Scope: The Chronic Condition Case Manager will have direct responsibility for managing an individual caseload using Complex and Chronic Condition Management constructs. This individual is expected to ...
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Apply Early
Lake Mary, FL · Remote
$62K - $74K/yr
Scope: The Chronic Condition Case Manager will have direct responsibility for managing an individual caseload using Complex and Chronic Condition Management constructs. This individual is expected to ...
Apply Early
Track PV milestones for multiple clinical programs and ensure timely sponsor review of safety documents (e.g., narratives, CIOMS/MedWatch forms). * Oversee documentation of operational decision ...
Track PV milestones for multiple clinical programs and ensure timely sponsor review of safety documents (e.g., narratives, CIOMS/MedWatch forms). * Oversee documentation of operational decision ...
Atlanta, GA · On-site
$142K - $188K/yr
... MedWatch and Biological Product Deviations. 6. Remains current trends in industry and practices up to and including association memberships with committee or work group participation. Identifies ...
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Apply Early
Atlanta, GA · On-site
$142K - $188K/yr
... MedWatch and Biological Product Deviations. 6. Remains current trends in industry and practices up to and including association memberships with committee or work group participation. Identifies ...
Apply Early
$153K - $202K/yr
... MedWatch and Biological Product Deviations. 6. Remains current trends in industry and practices up to and including association memberships with committee or work group participation. Identifies ...
New
$153K - $202K/yr
... MedWatch and Biological Product Deviations. 6. Remains current trends in industry and practices up to and including association memberships with committee or work group participation. Identifies ...
New
Newark, DE · On-site
$83K - $129K/yr
Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications. Skills: * Proven ability to independently collect, analyze, and ...
Newark, DE · On-site
$83K - $129K/yr
Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications. Skills: * Proven ability to independently collect, analyze, and ...
Newark, DE · On-site
$83K - $129K/yr
Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications. Skills: * Proven ability to independently collect, analyze, and ...
Newark, DE · On-site
$83K - $129K/yr
Awareness of regulatory reporting processes, including MedWatch reports, notified body communications, and external notifications. Skills: * Proven ability to independently collect, analyze, and ...
Lake Mary, FL · On-site +1
$62K - $74K/yr
Scope: The Chronic Condition Case Manager will have direct responsibility for managing an individual caseload using Complex and Chronic Condition Management constructs. This individual is expected to ...
Lake Mary, FL · On-site +1
$62K - $74K/yr
Scope: The Chronic Condition Case Manager will have direct responsibility for managing an individual caseload using Complex and Chronic Condition Management constructs. This individual is expected to ...
Write Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring timely transmission to the appropriate regulatory authorities. * Compose written communications ...
Write Medical Device Reports (MDRs), MedWatch, Vigilance, and other regulatory reports, ensuring timely transmission to the appropriate regulatory authorities. * Compose written communications ...
$8.89 - $13.70
16% of jobs
$15.17 is the 25th percentile. Wages below this are outliers.
$13.70 - $18.51
29% of jobs
The median wage is $19.71 / hr.
$18.51 - $23.32
19% of jobs
$27.58 is the 75th percentile. Wages above this are outliers.
$23.32 - $28.13
12% of jobs
$28.13 - $32.93
8% of jobs
$32.93 - $37.74
5% of jobs
$37.74 - $42.55
4% of jobs
$42.55 - $47.36
2% of jobs
$47.36 - $52.16
2% of jobs
$52.16 - $56.97
1% of jobs
$56.97 - $61.78
1% of jobs
$8
$26
$61
A MedWatch job typically involves monitoring, reviewing, and reporting adverse events, product complaints, and safety issues related to pharmaceuticals, medical devices, and other healthcare products. Professionals in this role ensure compliance with FDA regulations by processing and evaluating safety data received from healthcare providers, patients, and manufacturers. Their work helps identify potential risks and contributes to patient safety by facilitating timely regulatory reporting and proper risk management.
To thrive as a Medwatch professional—commonly involved in pharmacovigilance or medical device reporting—you need a strong background in healthcare, regulatory compliance, and detailed data analysis, often supported by a life sciences degree. Familiarity with MedWatch reporting systems, FDA safety databases, and adverse event tracking software is highly beneficial. Attention to detail, strong written communication, and the ability to work collaboratively under deadlines are important soft skills for this role. These competencies are vital for ensuring accurate adverse event reporting and compliance with regulatory standards, which helps protect patient safety and maintain healthcare quality.
A typical day in a Medwatch role involves reviewing and processing reports of adverse drug or device events, assessing the seriousness and validity of each case, and ensuring timely submission to regulatory authorities such as the FDA. You may collaborate with healthcare providers, quality assurance teams, and regulatory specialists to gather complete information and answer follow-up questions. Many Medwatch professionals also participate in data analysis and periodic safety reviews to identify potential safety signals. This position requires balancing analytical tasks with strong communication, as you both interpret data and relay critical safety information within your organization.
$56.75 - $68.25/hr
Other
Posted 25 days ago
Pharmacovigilance Pharmacist
Bring your clinical lens to the world of drug safety and reporting.
Key Responsibilities:
Qualifications:
Why Join Us?
