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Remote Pharmaceutical Project Manager Jobs in Mobile, AL

Medical Writing Manager

Mobile, AL · 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 ...

If remote from Atlanta or anywhere else, monthly travel to Calvert, Alabama for 2-3 day stay ... Strong project management and organizational skills * Excellent communication and stakeholder ...

... manages complex, large-scale customer engagements globally. This is a remote position for ... project management experience, with a minimum of 3 years in leadership roles managing teams and ...

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 ...

Showing results 21-40

Remote Pharmaceutical Project Manager information

See Mobile, AL salary details

$44.7K

$104.2K

$168.2K

How much do remote pharmaceutical project manager jobs pay per year?

As of Aug 20, 2026, the average yearly pay for remote pharmaceutical project manager in Mobile, AL is $104,220.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,400.00 and $127,500.00 per year, depending on experience, location, and employer.

What is the difference between Remote Pharmaceutical Project Manager vs Remote Pharmaceutical Sales Representative?

AspectRemote Pharmaceutical Project ManagerRemote Pharmaceutical Sales Representative
Required CredentialsProject management certification, life sciences degreeSales experience, pharmaceutical product knowledge
Work EnvironmentCollaborates with cross-functional teams, manages projects remotelyEngages with healthcare providers, promotes products remotely
Employer & Industry UsagePharmaceutical companies, biotech firmsPharmaceutical companies, medical device firms
Search & Comparison IntentProject management roles in pharmaSales roles in pharma

The Remote Pharmaceutical Project Manager focuses on overseeing drug development projects, coordinating teams, and ensuring timely delivery. In contrast, the Remote Pharmaceutical Sales Representative concentrates on promoting products to healthcare professionals and increasing sales. While both roles require industry knowledge, project managers emphasize coordination and planning, whereas sales reps focus on client engagement and sales targets.

What are popular job titles related to Remote Pharmaceutical Project Manager jobs in Mobile, AL?

For Remote Pharmaceutical Project Manager jobs in Mobile, AL, the most frequently searched job titles are:

What job categories do people searching Remote Pharmaceutical Project Manager jobs in Mobile, AL look for?

The top searched job categories for Remote Pharmaceutical Project Manager jobs in Mobile, AL are:

What cities near Mobile, AL are hiring for Remote Pharmaceutical Project Manager jobs?

Cities near Mobile, AL with the most Remote Pharmaceutical Project Manager job openings:

Infographic showing various Remote Pharmaceutical Project Manager job openings in Mobile, AL as of August 2026, with employment types broken down into 74% Full Time, 15% Part Time, and 11% Contract. Highlights an 100% Remote job distribution, with an average salary of $104,220 per year, or $50.1 per hour.

Medical Writing Manager

micro1 AI

Mobile, AL • 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.