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Remote Clinical Data Coding Jobs in Tucson, AZ (NOW HIRING)

micro1 AI

Clinical Pharmacy Technicians

Tucson, AZ · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... coding, seriousness and causality assessment, expectedness determination, and aggregate safety data ...

System One

Clinical Science Program Specialist

Oro Valley, AZ · Remote

$35 - $37/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Remote Hours : M-F 1st shift Compensation : $35.00 - $37.00/hr Type : Contract, Potential for ... Track and communicate project reports and clinical study data to Pharma and company clients.

System One

Clinical Science Program Specialist

Oro Valley, AZ · Remote

$35 - $37/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Remote Hours : M-F 1st shift Compensation : $35.00 - $37.00/hr Type : Contract, Potential for ... Track and communicate project reports and clinical study data to Pharma and company clients.

System One

Clinical Science Program Specialist

Oro Valley, AZ · Remote

$35 - $37/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Remote Work Model : Onsite Hours : M-F 1st shift Compensation : $35.00 - $37.00/hr Type : Contract ... Track and communicate project reports and clinical study data to Pharma and company clients.

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Showing results 21-40

All JobsClinical Data Coding JobsRemote Clinical Data Coding JobsRemote Clinical Data Coding Jobs in Tucson, AZ

Remote Clinical Data Coding information

See Tucson, AZ salary details

$18

$54

$77

How much do remote clinical data coding jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for remote clinical data coding in Tucson, AZ is $54.05, according to ZipRecruiter salary data. Most workers in this role earn between $42.74 and $64.33 per hour, depending on experience, location, and employer.

What is the difference between Remote Clinical Data Coding vs Remote Medical Billing and Coding?

AspectRemote Clinical Data CodingRemote Medical Billing and Coding
CredentialsCertification in Clinical Data Coding (e.g., CCS, CPC)Certification in Medical Billing and Coding (e.g., CPC, CBCS)
Work EnvironmentHealthcare facilities, research organizations, insurance companiesHospitals, clinics, insurance companies
Industry UsageClinical research, healthcare data managementPatient billing, insurance claims processing
Search IntentFocus on clinical data, research codingFocus on billing, claims, reimbursement

Remote Clinical Data Coding involves translating clinical research data into standardized codes for analysis, often requiring specific certifications. Remote Medical Billing and Coding focuses on processing insurance claims and patient billing. While both roles involve coding and certifications, they serve different functions within healthcare and are used in different settings.

What are popular job titles related to Remote Clinical Data Coding jobs in Tucson, AZ?

For Remote Clinical Data Coding jobs in Tucson, AZ, the most frequently searched job titles are:

What job categories do people searching Remote Clinical Data Coding jobs in Tucson, AZ look for?

The top searched job categories for Remote Clinical Data Coding jobs in Tucson, AZ are:

What cities near Tucson, AZ are hiring for Remote Clinical Data Coding jobs?

Cities near Tucson, AZ with the most Remote Clinical Data Coding job openings:

Remote Clinical Data Coding jobs near you
Infographic showing various Remote Clinical Data Coding job openings in Tucson, AZ as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 13% Part Time, and 4% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $112,426 per year, or $54.1 per hour.

Clinical Pharmacy Technicians

micro1 AI

Tucson, AZ • Remote

$70 - $80/hr

Part-time

Posted 16 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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