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Part Time Freelance Clinical Project Manager Jobs in Rochester, NY

micro1 AI

Medical Writing Manager

Rochester, NY · Remote

$50 - $80/hr

... customer's project focused on developing advanced AI-assisted writing tools for clinical ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

Monroe County, NY

Nurse Manager, prov.

Rochester, NY · On-site

$80K - $111K/yr

Work involves planning and implementing the clinical care of patients and nursing procedures for ... Eighteen (18) months paid full-time or its part-time equivalent experience as a Registered Nurse ...

footprint Solutions

Part Time Merchandiser

Bloomfield, NY · On-site

$16/hr

This position will report directly to a District Manager, but you will work independently onsite at ... projects in your area. • Opportunities to work close to home or (if willing) the opportunity to ...

footprint Solutions

Part Time Merchandiser

Rochester, NY · On-site

$16/hr

This position will report directly to a District Manager, but you will work independently onsite at ... projects in your area. • Opportunities to work close to home or (if willing) the opportunity to ...

Nutraco

REGIONAL Dietitian

Rochester, NY

$70K - $80K/yr

We offer full time and part time positions across with placements available in many states! Find ... Take direction from the VP of Clinical Services and Regional Clinical Director. * Provide ...

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All JobsClinical Project JobsPart Time Freelance Clinical Project Manager JobsPart Time Freelance Clinical Project Manager Jobs in Rochester, NY

Part Time Freelance Clinical Project Manager information

See Rochester, NY salary details

$28

$59

$106

How much do part time freelance clinical project manager jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for part time freelance clinical project manager in Rochester, NY is $59.89, according to ZipRecruiter salary data. Most workers in this role earn between $41.73 and $70.19 per hour, depending on experience, location, and employer.

What is the difference between Part Time Freelance Clinical Project Manager vs Part Time Freelance Clinical Research Associate?

AspectPart Time Freelance Clinical Project ManagerPart Time Freelance Clinical Research Associate
CredentialsTypically requires project management certifications and industry experienceOften requires clinical research certifications and monitoring experience
Work EnvironmentManages projects, coordinates teams, oversees timelinesMonitors clinical sites, ensures protocol compliance, collects data
Employer & Industry UsageUsed by biotech, pharma companies, CROs for project oversightCommonly employed by CROs, sponsors for site monitoring

While both roles are part-time and freelance within the clinical research industry, the Clinical Project Manager focuses on managing entire projects and teams, whereas the Clinical Research Associate primarily monitors clinical sites and data collection. Their certifications, daily tasks, and industry usage differ, making each role suited to different skill sets and responsibilities.

What are popular job titles related to Part Time Freelance Clinical Project Manager jobs in Rochester, NY? For Part Time Freelance Clinical Project Manager jobs in Rochester, NY, the most frequently searched job titles are:
What job categories do people searching Part Time Freelance Clinical Project Manager jobs in Rochester, NY look for? The top searched job categories for Part Time Freelance Clinical Project Manager jobs in Rochester, NY are:
What cities near Rochester, NY are hiring for Part Time Freelance Clinical Project Manager jobs? Cities near Rochester, NY with the most Part Time Freelance Clinical Project Manager job openings:
Part Time Freelance Clinical Project Manager jobs near you
Infographic showing various Part Time Freelance Clinical Project Manager job openings in Rochester, NY as of August 2026, with employment types broken down into 84% Full Time, 13% Part Time, and 3% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $124,578 per year, or $59.9 per hour.

Medical Writing Manager

micro1 AI

Rochester, NY • Remote

$50 - $80/hr

Part-time

Posted 8 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