2

Freelance Remote Risk Analyst Jobs in Mount Pleasant, SC

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... benefit-risk conclusions in alignment with best practices. * Assess template and structural ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... benefit-risk conclusions in alignment with best practices. * Assess template and structural ...

Conduct thorough financial analysis and risk assessment to evaluate the creditworthiness of loan applicants. Review financial statements, credit reports, and other relevant documents. * Loan ...

This position can be fully remote. GAI's Power Business Unit focuses on developing and supporting ... statistics to analyze risk in a complex engineering problem. Experience Required * 8+ years ...

Showing results 21-40

Freelance Remote Risk Analyst information

See Mount Pleasant, SC salary details

$14

$38

$62

How much do freelance remote risk analyst jobs pay per hour?

As of Aug 15, 2026, the average hourly pay for freelance remote risk analyst in Mount Pleasant, SC is $38.70, according to ZipRecruiter salary data. Most workers in this role earn between $28.51 and $47.12 per hour, depending on experience, location, and employer.

What is the difference between Freelance Remote Risk Analyst vs Freelance Remote Credit Analyst?

AspectFreelance Remote Risk AnalystFreelance Remote Credit Analyst
CredentialsRisk management certifications, analytical skillsFinancial analysis, credit risk certifications
Work EnvironmentRemote, project-based, consultingRemote, financial institutions, consulting
Employer & IndustryConsulting firms, finance, insuranceBanks, lending companies, financial services
Search & Comparison IntentRisk assessment, financial risk, consultingCredit evaluation, lending risk, financial analysis

Both roles involve financial analysis and risk assessment but differ in focus. A Freelance Remote Risk Analyst primarily evaluates overall risk factors for organizations, while a Freelance Remote Credit Analyst specializes in assessing creditworthiness for lending decisions. Understanding these distinctions helps freelancers target the right clients and projects.

Can a freelance remote risk analyst work remotely?

Yes, a freelance remote risk analyst can work remotely, as the role primarily involves analyzing data, assessing risks, and using tools like spreadsheets and risk management software, which can be done from any location with internet access. Remote work offers flexibility and often requires strong communication skills and relevant certifications such as FRM or CRM.

Are freelance remote risk analysts in demand?

Freelance remote risk analysts are in growing demand as companies seek flexible professionals to assess financial, operational, and cybersecurity risks. Strong analytical skills, industry certifications, and familiarity with risk management tools increase employability in this field.

What are popular job titles related to Freelance Remote Risk Analyst jobs in Mount Pleasant, SC?

For Freelance Remote Risk Analyst jobs in Mount Pleasant, SC, the most frequently searched job titles are:

What job categories do people searching Freelance Remote Risk Analyst jobs in Mount Pleasant, SC look for?

The top searched job categories for Freelance Remote Risk Analyst jobs in Mount Pleasant, SC are:

Infographic showing various Freelance Remote Risk Analyst job openings in Mount Pleasant, SC as of August 2026, with employment types broken down into 1% As Needed, 88% Full Time, 8% Part Time, and 3% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $80,489 per year, or $38.7 per hour.

Clinical Pharmacy Technicians

micro1 AI

Charleston, SC • Remote

$70 - $80/hr

Part-time

Posted 11 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.