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Content Risk Reviewer Jobs in Oregon (NOW HIRING)

Review and interpret clinical trial and post-marketing safety data. * Perform benefit-risk analyses ... Experience with content management systems preferred. Why Join Med Communications? Join a ...

$128K - $160K/yr

Owns operational workstreams that ensure Elevate runs smoothly, from logistics to content ... The role's risk level (low/moderate/high) is defined based on system and data access. * Other ...

Senior Manager, Policy & Governance

OR · On-site +1

$107K - $116K/yr

Upstart's Enterprise Risk Management team helps ensure Upstart Bank operates with a strong ... Oversee the end-to-end policy lifecycle, including policy reviews, approvals, exceptions, version ...

OR · On-site

$139K - $189K/yr

Review and help develop compelling yet compliant Marketing content * Collaborate with Finance and Risk functions to minimize loss, investigate fraud and create policies and process to reduce it

This role oversees QA, validation, and release of medical policy content prior to production ... Quality Assurance & Risk Management: Lead go/no-go decisions, validate testing (UAT), and establish ...

... content to be relevant to the account and audience * Review and approve Job Hazard Analyses (JHAs) submitted by technicians and engineers * Supervise high-risk work happening on site each day ...

Clinical Content Migration. Support migration of Design Decision Matrices (DDMs), Data Collection ... Risk and Quality Management. Identify, document, and track clinical and functional risks and issues ...

Scope of Work * Author and review evaluation tasks that require nuanced clinical judgment ... Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ...

Hematologist / Oncologist

Bend, OR · Remote

$160 - $200/hr

Scope of Work * Author and review evaluation tasks that require nuanced clinical judgment ... Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ...

Scope of Work * Author and review evaluation tasks that require nuanced clinical judgment ... Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ...

Track task assignments through initial development, performance, review, and feedback ... and risk mitigation * Effective organizational skills * Effective written and verbal English ...

... reviewing each for regulatory, fair lending, and disclosure risk, and approving marketing materials and third-party-produced content before release. * Regulatory review & approval: Bring UDAAP ...

Scope of Work * Author and review evaluation tasks that require nuanced clinical judgment ... Evaluate benefit-risk reasoning, scrutinizing the durability of conclusions in light of new events ...

Showing results 41-60

Content Risk Reviewer information

What is the difference between Content Risk Reviewer vs Content Moderator?

AspectContent Risk ReviewerContent Moderator
CredentialsTypically requires familiarity with content policies, risk assessment, and sometimes certifications in compliance or content reviewOften requires knowledge of platform policies, communication skills, and sometimes basic certifications in social media or content management
Work EnvironmentUsually in office or remote settings, analyzing flagged content for potential risks or violationsPrimarily in social media, forums, or online platforms, monitoring live or flagged content
Employer & IndustryTech companies, social media platforms, online marketplacesSocial media companies, online forums, content sharing platforms

While both roles involve reviewing online content, Content Risk Reviewers focus on assessing potential risks and compliance issues, whereas Content Moderators primarily enforce platform policies by removing or flagging inappropriate content. The roles often overlap but differ in scope and focus.

How do you become a content risk reviewer?

To become a content risk reviewer, candidates typically need strong analytical skills, knowledge of content policies, and experience with content moderation tools. Relevant qualifications may include a high school diploma or higher, familiarity with online platforms, and the ability to evaluate potentially harmful or inappropriate content efficiently.
What are popular job titles related to Content Risk Reviewer jobs in Oregon? For Content Risk Reviewer jobs in Oregon, the most frequently searched job titles are:
What job categories do people searching Content Risk Reviewer jobs in Oregon look for? The top searched job categories for Content Risk Reviewer jobs in Oregon are:
What cities in Oregon are hiring for Content Risk Reviewer jobs? Cities in Oregon with the most Content Risk Reviewer job openings:
Infographic showing various Content Risk Reviewer job openings in Oregon as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Full-time

Posted 10 days ago


Job description

Pharmacovigilance Physician
Location: Remote (United States)
Department: Pharmacovigilance
Reports To: Global Head of Pharmacovigilance and Drug Safety
Employment Type: Contractor
Join our Team
Med Communications is seeking a Pharmacovigilance Physician (MD, DO, or equivalent) to provide medical expertise in the evaluation and interpretation of safety data for pharmaceutical products. This role is responsible for medical review of individual case safety reports, aggregate safety assessments, signal detection activities, benefit-risk evaluations, and support of regulatory safety reporting requirements. The Pharmacovigilance Physician serves as a key medical resource for client safety activities and collaborates with clients, regulatory authorities, and internal teams to support pharmacovigilance compliance and patient safety.
What You'll Do
As our Pharmacovigilance Physician Contractor you will:
Safety Review and Medical Assessment
  • Conduct medical review of individual case safety reports (ICSRs) and provide medical assessment statements.
  • Review and interpret clinical trial and post-marketing safety data.
  • Perform benefit-risk analyses and medical assessments for client products.
  • Evaluate aggregate safety information for periodic safety reports and ad hoc requests.
  • Support safety signal detection, evaluation, and verification activities.
Pharmacovigilance Support
  • Support pharmacovigilance systems for Med Communications and client programs in accordance with contractual requirements.
  • Integrate regulatory and compliance requirements into medical assessment activities.
  • Assist and support the Qualified Person for Pharmacovigilance (QPPV), as required.
Client and Regulatory Collaboration
  • Lead and participate in client safety meetings.
  • Provide medical expertise during interactions with safety monitoring boards and regulatory authorities.
  • Represent client interests in safety-related discussions when appropriate.
Medical and Regulatory Documentation
  • Assist in drafting, reviewing, and refining medical sections of:
    • Periodic Adverse Drug Experience Reports (PADERs)
    • Periodic Safety Update Reports (PSURs)
    • Development Safety Update Reports (DSURs)
    • Periodic Benefit-Risk Evaluation Reports (PBRERs)
    • IND Annual Reports
    • Investigator's Brochures (IBs)
    • Integrated Summary of Safety (ISS) documents
    • U.S. and international product labeling documents
    • Regulatory authority safety information requests
  • Assist with drafting, reviewing, and refining risk management plans and risk evaluation and mitigation strategies when required by client contracts.
What We're Looking For
Education
Either:
  • Licensed Medical Physician (MD, DO, or equivalent) in good standing in applicable state(s) of licensure. Board certification in a therapeutic area relevant to client programs is preferred.
Or:
  • Unlicensed Medical Physician (MD, DO, or equivalent) with no record of past or present Medical Board disciplinary action and at least five (5) years of combined pharmacovigilance experience, clinical healthcare provider experience, or equivalent experience.
Preferred:
  • Degree or training in Epidemiology.
Experience
  • Minimum of five (5) years of pharmacovigilance experience in the pharmaceutical industry or equivalent experience, including:
    • Clinical trials investigator
    • Health authority inspector
    • Epidemiologist
    • Other related healthcare or drug safety roles
Knowledge, Skills, and Abilities
Technical Knowledge
  • Understanding of pharmacovigilance regulations and compliance requirements from:
    • U.S. Food and Drug Administration (FDA)
    • European Medicines Agency (EMA)
    • Japan Pharmaceuticals and Medical Devices Agency (PMDA)
    • United Kingdom Medicines and Healthcare products Regulatory Agency (MHRA)
    • International Council for Harmonisation (ICH)
Computer Skills
  • Proficiency with Microsoft Office applications preferred.
  • Experience with content management systems preferred.
Why Join Med Communications?
Join a collaborative team dedicated to supporting clients with high-quality pharmacovigilance services and maintaining a strong commitment to patient safety, regulatory compliance, and scientific excellence.
Med Communications is an Equal Opportunity Employer and is committed to fostering a diverse and inclusive workplace.