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Part Time Remote Clinical Data Coordinator Jobs in Rochester, NY

Talkiatry

Psychiatrist - Part Time/Full Time

Rochester, NY · Remote

$325K - $375K/yr

Minimal administrative burden in a fully remote, outpatient model What your day-to-day practice ... coordination, and licensing Clinical autonomy & flexibility: * Control over schedule and weekly ...

Talkiatry

Psychiatrist - Part Time/Full Time

Rochester, NY · Remote

$325K - $375K/yr

Minimal administrative burden in a fully remote, outpatient model What your day-to-day practice ... coordination, and licensing Clinical autonomy & flexibility: * Control over schedule and weekly ...

micro1 AI

Director of Biostatistics

Rochester, NY · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... missing data handling in alignment with the statistical analysis plan (SAP). * Identify ...

micro1 AI

Biostatistician

Rochester, NY · Remote

$60 - $65/hr

Remote micro1 is engaging Biostatisticians to contribute their clinical statistics expertise to a ... missing data handling in alignment with the statistical analysis plan (SAP). * Identify ...

micro1 AI

Director of Biostatistics

Rochester, NY · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Source, construct, and curate authentic datasets including trial data, patient records, and ...

micro1 AI

Biostatistician

Rochester, NY · Remote

$60 - $100/hr

Remote micro1 is engaging Biostatisticians to contribute to a customer's advanced project in AI ... Source, construct, and curate authentic datasets including trial data, patient records, and ...

micro1 AI

Medical Billing Specialist

Rochester, NY · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... source data. * Exceptional written and verbal communication skills, especially in providing ...

micro1 AI

Medical Writing Manager

Rochester, NY · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... source data. * Exceptional written and verbal communication skills, especially in providing ...

Pronexus, LLC

Senior Accountant

Rochester, NY · Remote

$68K - $85K/yr

Senior Accountant *Part-Time or Full-Time, Remote, On-Site, and Hybrid Opportunities Available ... Review and analyze financial data to identify variances and discrepancies, resolving issues ...

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Showing results 21-37

All JobsClinical Data JobsPart Time Remote Clinical Data Coordinator JobsPart Time Remote Clinical Data Coordinator Jobs in Rochester, NY

Part Time Remote Clinical Data Coordinator information

See Rochester, NY salary details

$15

$29

$56

How much do part time remote clinical data coordinator jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for part time remote clinical data coordinator in Rochester, NY is $29.25, according to ZipRecruiter salary data. Most workers in this role earn between $22.55 and $33.46 per hour, depending on experience, location, and employer.

What is the difference between Part Time Remote Clinical Data Coordinator vs Part Time Remote Clinical Research Associate?

AspectPart Time Remote Clinical Data CoordinatorPart Time Remote Clinical Research Associate
CredentialsTypically requires a degree in health, life sciences, or related field; certifications like CDISC or data management certifications are commonRequires a degree in health sciences or related; often holds certifications like CCRP or RAC
Work EnvironmentPrimarily data entry, management, and validation in clinical trial settingsMonitoring clinical sites, ensuring protocol compliance remotely
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and biotech firms for data management rolesEmployed by similar organizations for overseeing trial progress and compliance

While both roles support clinical trials remotely, the Clinical Data Coordinator focuses on managing and validating trial data, whereas the Clinical Research Associate oversees site activities and ensures protocol adherence. Both roles require related certifications and are integral to remote clinical trial operations.

What are the most commonly searched types of Part Time Remote Clinical Data jobs in Rochester, NY?

The most popular types of Part Time Remote Clinical Data jobs in Rochester, NY are:

What are popular job titles related to Part Time Remote Clinical Data Coordinator jobs in Rochester, NY?

For Part Time Remote Clinical Data Coordinator jobs in Rochester, NY, the most frequently searched job titles are:

What job categories do people searching Part Time Remote Clinical Data Coordinator jobs in Rochester, NY look for?

The top searched job categories for Part Time Remote Clinical Data Coordinator jobs in Rochester, NY are:

What cities near Rochester, NY are hiring for Part Time Remote Clinical Data Coordinator jobs?

Cities near Rochester, NY with the most Part Time Remote Clinical Data Coordinator job openings:

Part Time Remote Clinical Data Coordinator jobs near you
Infographic showing various Part Time Remote Clinical Data Coordinator job openings in Rochester, NY as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 85% Physical, 4% Hybrid, and 11% Remote job distribution, with an average salary of $60,844 per year, or $29.3 per hour.

Medical Writer / Clinical Document Author

micro1 AI

Rochester, NY • Remote

$50 - $80/hr

Part-time

Posted 16 days ago

Job description

Role Title: Medical Writer / Clinical Document Author


Role Type: Contractor


Location: Remote


micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer’s project focused on developing advanced AI-assisted writing tools for clinical documentation. 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.


Scope of Work

  1. Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  2. Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  3. Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  4. Trace narrative claims to source records—tables, figures, listings, and protocols—to verify that all assertions are appropriately supported.
  5. Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  6. Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.


Preferred Qualifications

  1. Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  2. Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  3. Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  4. Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  5. Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  6. Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  7. Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.


Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents — through your expert input, judgment, and real-world experience.

Apply