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Remote Intern Pmp Project Manager Jobs in Gray, GA

Medical Writing Manager

Macon, GA · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Collaborate with project leads to refine evaluation frameworks and document best practices for ...

This position is eligible to be fully remote or for work out of our Lexington, KY HQ or our ... Working closely with VDC project managers, engineers, supers and construction PMs to ensure ...

Project & Process Management • Lead issue-resolution activities during early-stage customer ... IFS experience is an asset. • Ability to travel regularly throughout the territory. • Remote ...

Enjoy the flexibility of remote work and the freedom to set your own schedule. This is an ... You'll be able to choose which projects you want to work on and when * You work on your own ...

Enjoy the flexibility of remote work and the freedom to set your own schedule. This is an ... You'll be able to choose which projects you want to work on and when * You work on your own ...

Enjoy the flexibility of remote work and the freedom to set your own schedule. This is an ... You'll be able to choose which projects you want to work on and when * You work on your own ...

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Collaborate with project leads to refine evaluation frameworks and document best practices for ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... customer project. In this role, you'll apply your expertise to help train next-generation AI ...

Pharmacovigilance Expert

Macon, GA · Remote

$70 - $80/hr

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... customer project. In this role, you'll apply your expertise to help train next-generation AI ...

Showing results 21-40

Remote Intern Pmp Project Manager information

See Gray, GA salary details

$18.5K

$31.9K

$43.1K

How much do remote intern pmp project manager jobs pay per year?

As of Aug 15, 2026, the average yearly pay for remote intern pmp project manager in Gray, GA is $31,888.00, according to ZipRecruiter salary data. Most workers in this role earn between $27,800.00 and $32,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Intern Pmp Project Manager vs Remote Junior Project Coordinator?

AspectRemote Intern Pmp Project ManagerRemote Junior Project Coordinator
CertificationsPMP certification preferred, or in progressNo certification required
Work EnvironmentRemote, managing projects, coordinating teamsRemote, supporting project tasks, assisting coordinators
Industry UsageCommon in project management roles across industriesEntry-level support role in project teams

The Remote Intern Pmp Project Manager typically has some project management training or certification and takes on responsibilities like planning and overseeing projects remotely. The Remote Junior Project Coordinator is an entry-level role focused on supporting project activities without requiring PMP certification. While both roles work remotely and support project teams, the Project Manager role involves more responsibility and leadership, whereas the Coordinator role emphasizes assistance and coordination tasks.

What job categories do people searching Remote Intern Pmp Project Manager jobs in Gray, GA look for?

The top searched job categories for Remote Intern Pmp Project Manager jobs in Gray, GA are:

What cities near Gray, GA are hiring for Remote Intern Pmp Project Manager jobs?

Cities near Gray, GA with the most Remote Intern Pmp Project Manager job openings:

Infographic showing various Remote Intern Pmp Project Manager job openings in Gray, GA as of July 2026, with employment types broken down into 81% Full Time, 10% Part Time, and 9% Contract. Highlights an 100% Remote job distribution, with an average salary of $31,888 per year, or $15.3 per hour.

Medical Writing Manager

micro1 AI

Macon, GA • Remote

$50 - $80/hr

Part-time

Posted 11 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.