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Content Risk Reviewer Jobs in Orlando, FL (NOW HIRING)

Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and ... benefit-risk conclusions in alignment with best practices. * Assess template and structural ...

Design-Build Pursuit Specialist

Orlando, FL · Hybrid

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This dynamic role engages in large, complex high-risk pursuits and supports a wide range of design ... Review, proofread, and edit proposals for clarity and grammar * Maintain and update databases and ...

Compounding Pharmacy Technician

Lake Mary, FL · On-site

$17 - $21/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... risk sterile products, and filling patient orders under the supervision of a pharmacist. The ... Access and review MSDS information when working with hazardous or non-hazardous chemicals to ensure ...

Compounding Pharmacy Technician

Lake Mary, FL · On-site

$17 - $21/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... risk sterile products, and filling patient orders under the supervision of a pharmacist. The ... Access and review MSDS information when working with hazardous or non-hazardous chemicals to ensure ...

Ensures all other reviews are conducted on a timely basis. * Creates an environment that fosters ... Open Door, Diversity in the Workplace) and maintenance of a risk-free environment. * Manages the ...

Ensures all other reviews are conducted on a timely basis. * Creates an environment that fosters ... Open Door, Diversity in the Workplace) and maintenance of a risk-free environment. * Manages the ...

Aechelon Technology, Inc. is a leading producer of 3D simulator content, including Geospecific ... Acts as a technical point of contact for quality risk and testability discussions. • Own large ...

Showing results 21-40

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 I become a content risk reviewer?

To become a content risk reviewer, candidates typically need strong critical thinking skills, knowledge of platform policies, and experience with content moderation tools. Relevant qualifications often include a high school diploma or equivalent, and some roles may require familiarity with content management systems or basic understanding of online safety. Training is usually provided by the employer to ensure adherence to specific guidelines and standards.

What are popular job titles related to Content Risk Reviewer jobs in Orlando, FL?

For Content Risk Reviewer jobs in Orlando, FL, the most frequently searched job titles are:

What job categories do people searching Content Risk Reviewer jobs in Orlando, FL look for?

The top searched job categories for Content Risk Reviewer jobs in Orlando, FL are:

What cities near Orlando, FL are hiring for Content Risk Reviewer jobs?

Cities near Orlando, FL with the most Content Risk Reviewer job openings:

Infographic showing various Content Risk Reviewer job openings in Orlando, FL as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 10% Part Time, and 3% Contract. Highlights an 89% Physical, 4% Hybrid, and 7% Remote job distribution.

Pharmacovigilance Expert

micro1 AI

Orlando, FL • Remote

$70 - $80/hr

Part-time

Posted 14 days ago


Job description

Role Title: Pharmacovigilance Expert


Role Type: Contractor


Location: Remote


micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety expertise on a key customer project. In this role, you'll apply your expertise to help train next-generation AI systems. Your work will shape how models learn, reason, and perform through high-quality, real-world input. No prior experience in AI is required — your domain knowledge is what matters. This opportunity is ideal for professionals experienced in authoring and reviewing complex safety reports, passionate about data quality, and committed to clear written and verbal communication.


Scope of Work

  1. Author and review evaluation tasks based on DSURs, PSURs/PBRERs, and associated safety data and case-level records.
  2. Apply expert judgment to assess the accuracy and adequacy of interval safety findings, signal evaluations, and benefit-risk conclusions in alignment with best practices.
  3. Assess template and structural conformity to ICH E2F and ICH E2C requirements, including proper section content, presentation of cumulative versus interval data, and completeness of appendices.
  4. Reconcile figures and case counts across report sections and data sources, identifying and documenting discrepancies significant for regulatory review.
  5. Evaluate safety conclusions in light of new data or events, and provide clear, structured written rationales supporting your determinations.
  6. Deliver structured feedback to inform the development of AI-driven tools for pharmacovigilance documentation and analysis.


Preferred Qualifications

  1. 5+ years of pharmacovigilance or drug safety experience at a sponsor, CRO, or as an independent consultant.
  2. Demonstrated proficiency in authoring or reviewing DSURs and/or PSURs/PBRERs from start to finish.
  3. Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and benefit-risk assessment methodology.
  4. Hands-on experience with MedDRA coding, seriousness and causality assessment, expectedness determination, and aggregate safety data analysis.
  5. Expertise in reconciling aggregate safety data and identifying inconsistencies with case-level information.
  6. Advanced degree in life sciences, pharmacy, nursing, or medicine (PharmD, MD, MSc, or equivalent).
  7. Experience in both development-stage and post-marketing safety reporting, QPPV or deputy QPPV roles, safety committee participation, or AI-assisted safety review tools is a plus.