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Full Time Sop Writing Jobs (NOW HIRING)

Customs Specialist - Entry Writer Time Type: Full Time The Entry Writer is responsible for the ... on client SOP, product service level and/or country and government agency requirements • ...

Technical Writer I

Austin, TX · On-site

$3.3K - $3.8K/mo

... writing customer service responses highly preferred. - Experience developing SOP and training ... year of full-time experience in technical writing, journalism, or communications work may be ...

Technical Writer I

Austin, TX · On-site

$3.3K - $3.8K/mo

... writing customer service responses highly preferred. - Experience developing SOP and training ... year of full-time experience in technical writing, journalism, or communications work may be ...

Job Type Full-time Description If you are looking for an exciting career opportunity in the ... Bachelor's degree in English, Communications, Technical Writing, or related field * Microsoft ...

Work with ELES staff to create standard operating procedures (SOP)s for elevator and escalator ... Experience in technical writing for standards, rules, standard operating procedures (SOPs), and ...

Work with ELES staff to create standard operating procedures (SOP)s for elevator and escalator ... Experience in technical writing for standards, rules, standard operating procedures (SOPs ...

Principal Medical Writer

$119K - $159K/yr

This position is also responsible for mentoringjuniorMWs (full-time employees and/or contractors ... Document Writing: * Managesthe assigned writing tasks and ensuresthatthe documents adhere ...

Fulltime, On-site, Quantico, VA; limited travel as required ( Role Overview: The Technical Writer ... All work supports the MSTP Quarterly Work Plan and Doctrine SOP, contributing to the ...

Showing results 21-40

Full Time Sop Writing information

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$13

$38

$66

How much do full time sop writing jobs pay per hour?

As of Aug 17, 2026, the average hourly pay for full time sop writing in the United States is $38.94, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $47.12 per hour, depending on experience, location, and employer.

What is a full time SOP writing job?

Full Time SOP (Standard Operating Procedure) Writing jobs involve creating detailed, step-by-step documents that outline how specific tasks or processes should be carried out within an organization. These roles require strong writing and organizational skills, as SOP writers must ensure clarity, compliance, and consistency in their documentation. Full-time SOP writers may collaborate with subject matter experts and various departments to accurately capture procedures and maintain updated documentation. The goal is to help organizations improve efficiency, quality, and safety by providing clear instructions for employees.

What are the key skills and qualifications needed to thrive as a full time SOP writer?

To thrive as a Full-Time SOP Writer, you need strong technical writing skills, attention to detail, and a background in the relevant industry or subject matter. Familiarity with documentation tools such as Microsoft Word, Google Docs, and document management systems, as well as knowledge of regulatory standards, is typically required. Excellent communication, organizational skills, and the ability to collaborate with subject matter experts make someone stand out in this position. These skills ensure the creation of clear, compliant, and effective SOPs that support operational consistency and quality within an organization.

What are some common challenges faced by professionals in a full time SOP writing role, and how can they overcome them?

One common challenge for full-time SOP writers is ensuring clarity and consistency across documents, especially when collaborating with different departments that have unique processes and terminology. Maintaining up-to-date procedures in a dynamic work environment can also be demanding, as processes may change frequently. To overcome these challenges, SOP writers should establish regular communication with subject matter experts, use standardized templates, and implement a robust review process to ensure accuracy and alignment. Leveraging document management tools can also help track revisions and streamline updates.

What is the difference between Full Time Sop Writing vs Technical Writer?

AspectFull Time Sop WritingTechnical Writer
CredentialsRelevant writing experience, industry-specific knowledgeDegree in technical communication, engineering, or related field
Work EnvironmentOffice or remote, focused on SOP documentationOffice or remote, creating manuals, guides, and documentation
Industry UsageCommon in manufacturing, healthcare, and quality assuranceUsed across IT, engineering, and product development sectors
Search & Comparison IntentPeople seeking SOP-specific roles or freelance SOP writingPeople comparing technical documentation roles or careers

Full Time SOP Writing focuses specifically on creating standard operating procedures within various industries, requiring specialized knowledge of processes and compliance. Technical Writers have a broader scope, producing manuals, guides, and documentation across multiple fields. While both roles involve technical writing skills, SOP writers concentrate on procedural documentation, whereas technical writers handle diverse technical content.

How to become a full time sop writer?

To become a full-time SOP (Standard Operating Procedure) writer, develop strong writing and technical skills, gain experience in process documentation, and build a portfolio of sample SOPs. Familiarity with industry standards, attention to detail, and proficiency with word processing tools are essential. Some professionals pursue certifications in technical writing to enhance credibility and job prospects.
More about Full Time Sop Writing jobs

What are the most commonly searched types of Sop Writing jobs?

The most popular types of Sop Writing jobs are:

What job categories do people searching Full Time Sop Writing jobs look for?

The top searched job categories for Full Time Sop Writing jobs are:

Infographic showing various Full Time Sop Writing job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 73% Full Time, 23% Part Time, and 3% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $81,001 per year, or $38.9 per hour.

$146K - $197K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 25 days ago


Job description

OVERVIEW:
The Senior Manager, Medical Writing will collaborate with project teams on the development of clinical documents in accordance with all applicable regulations, Good Clinical Practices, and Standard Operating Procedures (SOPs) and will oversee the work of contract writers on the clinical program.
RESPONSIBILITIES:
• Produce high quality and on-time writing deliverables
• Independently plan, write, edit, and format key documents, including clinical protocols, investigator brochures, clinical study reports, integrated safety and efficacy summaries and related documents
• Facilitate/manage efficient review and finalization process for documents produced internally and/or externally by consultants, contractors and vendors
• Represent Medical Writing on multiple early phase project teams or on specific late phase project teams and collaborate with the Director of Medical Writing to ensure proper planning and resourcing for upcoming project writing deliverables
• Collaborate effectively with Biometrics, Clinical Operations, Clinical Development, Regulatory Affairs, Pre-Clinical Development, Program Management, Research, Quality, and Corporate Communications, as well as with external stakeholders
• Serve as subject matter expert for clinical documents and their production
• Contribute to SOP and template development and maintenance
QUALIFICATIONS:
• Bachelor's degree in Life Science with relevant writing expertise or in English/Communications with relevant science expertise; advanced degree and/or professional certification/credentials preferred
• 6+ years of experience as a medical writer in the sponsor and/or CRO setting; experience with regulatory submissions (CTA/IND/NDA/BLA) and knowledge of eCTD formatting is a plus
• In-depth knowledge of Good Clinical Practices, FDA regulations, ICH guidelines, and the drug development process
• Successful track record of managing multiple projects in a fast-paced and deadline-driven environment with impeccable attention to detail and ability to complete writing assignments in a timely manner
• Experience overseeing the work of contract writers is a plus; must be proficient with Microsoft Windows, Word, Excel, and PowerPoint
• Ability to travel approximately 10% is required; demonstrate clear alignment with Alnylam Core Values including Commitment to People, Fiercely Innovative, Purposeful Urgency, Open Culture, and Passion for Excellence
#LI-JB1 #Remote
U.S. Pay Range
$146,100.00 - $197,700.00
The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Base pay will be determined based on a number of factors including, but not limited to, relevant experience, skills, and education. This role is eligible for an annual short-term incentive award (e.g., bonus or sales incentive) and an annual long-term incentive award (e.g., equity).
Alnylam's robust Total Rewards package is designed to support your overall health and well-being. We offer comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match. Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks. We also offer generous family resources and leave. Our commitment to your well-being reflects our belief that caring for our people fuels the impact we create together.
Learn more about these and additional benefits offered by Alnylam by visiting the Benefits section of the Careers website: https://www.alnylam.com/careers
About Alnylam
We are the leader in RNAi therapeutics - a revolutionary approach with the potential to transform the lives of people with rare and common diseases. Built on Nobel Prize-winning science, Alnylam has delivered the breakthroughs that made RNAi therapeutics possible and are just at the beginning of what's possible. Our deep pipeline, late-stage programs, and bold vision reflect our core values: fierce innovation, passion for excellence, purposeful urgency, open culture and commitment to people. We're proud to be a globally recognized top employer, where an authentic, inclusive culture and breakthrough thinking fuel one another.
At Alnylam, we commit to an inclusive recruitment process and equal employment opportunity. Qualified applicants will receive consideration for employment without regard to their sex, gender or gender identity, sexual orientation, race, color, ethnicity, national origin, ancestry, citizenship, religion, creed, physical or mental disability, pregnancy status or related conditions, genetic information, veteran or military status, marital or familial status, political affiliation, age, or any other factor protected by federal, state, or local law. Alnylam is an E-Verify Employer.