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Remote Process Safety Manager Jobs in Midland, TX

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion ...

Membership Sales Manager - Odessa, TX

Odessa, TX · On-site +1

$75K - $180K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Hybrid (90% field-based within the market; 10% remote) Candidate must live within 50 to 75 miles of ... Sales Process Management: Sales Manager will manage the full sales cycle from initial outreach to ...

Foreman

Midland, TX · On-site +1

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Job Summary We are seeking an experienced and safety driven General Foreman to join our team for ... process - it is probably fraudulent. Geographic Disclosure Remote oilfield and/or plant operations.

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and ...

Remote micro1 is engaging Pharmacovigilance Experts to contribute their advanced drug safety ... Working fluency with ICH E2F, ICH E2C(R2), and GVP guidelines, including signal management and ...

Remote micro1 is engaging Chemistry Specialists to participate in a project supporting a leading ... process optimization. * Design and interpret complex laboratory experiments involving chemical ...

Remote micro1 is engaging Chemistry Specialists to participate in a project supporting a leading ... process optimization. * Design and interpret complex laboratory experiments involving chemical ...

Showing results 21-40

Remote Process Safety Manager information

See Midland, TX salary details

$33.4K

$99.9K

$163.5K

How much do remote process safety manager jobs pay per year?

As of Aug 20, 2026, the average yearly pay for remote process safety manager in Midland, TX is $99,880.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,200.00 and $127,100.00 per year, depending on experience, location, and employer.

What is the difference between Remote Process Safety Manager vs Remote Process Engineer?

AspectRemote Process Safety ManagerRemote Process Engineer
Required CertificationsPE, CSP, or similar safety certificationsPE, engineering licenses, technical certifications
Work EnvironmentFocus on safety protocols, risk assessments, complianceDesign, optimize, and troubleshoot processes
Industry UsageCommon in safety-critical industries like oil & gas, chemicalsUsed across manufacturing, chemical, and energy sectors

The Remote Process Safety Manager primarily focuses on safety management, risk mitigation, and regulatory compliance, requiring safety-specific certifications. In contrast, the Remote Process Engineer concentrates on process design and optimization, often with engineering licenses. Both roles are vital in safety-critical industries but serve different functions within process operations.

What are popular job titles related to Remote Process Safety Manager jobs in Midland, TX?

For Remote Process Safety Manager jobs in Midland, TX, the most frequently searched job titles are:

What job categories do people searching Remote Process Safety Manager jobs in Midland, TX look for?

The top searched job categories for Remote Process Safety Manager jobs in Midland, TX are:

What cities near Midland, TX are hiring for Remote Process Safety Manager jobs?

Cities near Midland, TX with the most Remote Process Safety Manager job openings:

Infographic showing various Remote Process Safety Manager job openings in Midland, TX as of June 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $99,880 per year, or $48 per hour.

Medical Writing Manager

micro1 AI

Midland, TX • 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.