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Remote Computer Assisted Ordering Technician Jobs in Kentucky

King's Daughters

Medication History Technician

Ashland, KY · On-site +1

$14 - $17/hr

... admission orders. • Discusses high-alert or targeted medications with the pharmacist as ... at a computer workstation for extended periods of time; regular performance of tasks with ...

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All JobsComputer Assisted Ordering Technician JobsRemote Computer Assisted Ordering Technician JobsRemote Computer Assisted Ordering Technician Jobs in Kentucky

Remote Computer Assisted Ordering Technician information

What is the difference between Remote Computer Assisted Ordering Technician vs Remote Medical Billing Specialist?

AspectRemote Computer Assisted Ordering TechnicianRemote Medical Billing Specialist
CredentialsBasic computer skills, training in ordering systemsMedical coding certification, billing training
Work EnvironmentHome office, healthcare or retail settingsHome-based, healthcare facilities or insurance companies
Industry UsageRetail, healthcare, pharmacyHealthcare, insurance
Common Search IntentOrdering process, system trainingBilling procedures, coding

The Remote Computer Assisted Ordering Technician focuses on processing orders using specialized systems, often in retail or healthcare settings, requiring basic technical skills. In contrast, the Remote Medical Billing Specialist handles medical billing and coding, requiring healthcare-specific certifications. Both roles are remote, but they serve different functions within the healthcare and retail industries.

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Remote Computer Assisted Ordering Technician jobs near you

Clinical Pharmacy Technicians

micro1 AI

Lexington, KY • 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.

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