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Documentation Lead Jobs (NOW HIRING)

Corning

Technical Documentation Lead

Wilmington, NC · On-site

Driving adoption of documentation standards and best practices across engineering and manufacturing teams * Building and expanding documentation capabilities over time, including tools, processes ...

Corning

Technical Documentation Lead

Wilmington, NC · Hybrid

Driving adoption of documentation standards and best practices across engineering and manufacturing teams * Building and expanding documentation capabilities over time, including tools, processes ...

Ascension

Lead Clinical Documentation Specialist

$96K/yr

The Lead Clinical Document Specialist (CDS) - Rapid Response serves as a high-level clinical documentation integrity expert, deployed to address urgent, complex, or high-impact issues across the CDI ...

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Documentation Lead information

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$30K

$156.3K

$206K

How much do documentation lead jobs pay per year?

As of Aug 3, 2026, the average yearly pay for documentation lead in the United States is $156,348.00, according to ZipRecruiter salary data. Most workers in this role earn between $116,000.00 and $205,000.00 per year, depending on experience, location, and employer.

How much do document specialists make in the US?

Document specialists in the US typically earn between $40,000 and $65,000 annually, depending on experience, location, and industry. Senior or specialized roles may pay higher, especially for those with skills in technical writing, document management software, or compliance standards.

What does a documentation staff do?

A documentation staff member is responsible for creating, editing, and maintaining clear and accurate technical documents, such as user manuals, guides, and procedures. They often use tools like MS Word or Adobe FrameMaker and ensure that documentation meets quality standards and is accessible to users and team members.

What is the difference between Documentation Lead vs Technical Writer?

AspectDocumentation LeadTechnical Writer
CredentialsTypically requires experience in technical communication, project management, and industry-specific knowledgeUsually requires a degree in technical communication, journalism, or related fields; certifications like STC are common
Work EnvironmentLeads teams, manages documentation projects, collaborates with multiple departmentsCreates and edits technical content, often working independently or within a small team
Industry UsageUsed in large organizations, especially in tech, engineering, and manufacturing sectorsCommon across various industries including IT, engineering, and healthcare

The main difference is that a Documentation Lead oversees documentation projects and manages teams, while a Technical Writer focuses on creating and editing technical content. The Documentation Lead has broader responsibilities, including project management, whereas the Technical Writer specializes in content development.

What kind of jobs in media bring in $150,000 a year?

In media, high-paying roles such as senior editors, media directors, or content strategists can earn $150,000 or more annually, especially with extensive experience and leadership responsibilities. These positions often require strong project management skills, industry knowledge, and advanced tools like Adobe Creative Suite or content management systems.

What degree do you need to be a documentation specialist?

A documentation lead typically holds a bachelor's degree in fields such as technical communication, English, journalism, or related areas. Relevant skills include proficiency with documentation tools like MadCap Flare or Adobe FrameMaker, and experience in technical writing or content management systems can enhance job prospects.
What job categories do people searching Documentation Lead jobs look for? The top searched job categories for Documentation Lead jobs are:
Documentation Lead jobs near you
Infographic showing various Documentation Lead job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 70% Full Time, 26% Part Time, and 3% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $156,348 per year, or $75.2 per hour.

Clinical Documentation Lead

Genentech

South San Francisco, CA • On-site

$113K - $211K/yr

Full-time

Posted 6 days ago

Genentech rating

8.8

Company rating: 8.8 out of 10

Based on 22 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical

Job description

We advance science so that we all have more time with the people we love.

Become a part of Genentech's Early Clinical Development team, working to bring pioneering therapies to patients. As a Clinical Documentation Lead in the Medical Communications Group, you will lead medical writing, editing, and project management for the development of clinical documents, including study protocols, informed consent forms, abstracts, manuscripts, and key scientific statements. You will partner closely with cross-functional stakeholders across the Roche organization, including colleagues in Clinical Science, Safety Science, Regulatory, and Clinical Operations.

The Opportunity:

  • Oversee the development of clinical protocols, informed consent forms, and other documents by creating and maintaining project timelines; ensuring adherence to internal templates and style guides; writing and editing; coordinating authoring teams and review cycles; managing adjudication of review comments; and coordinating publishing, signoff, and archiving

  • Act as a key strategic thinking partner for Clinical Scientists and study teams to align document deliverables with clinical goals

  • Acquire and demonstrate a deep understanding of the drug development process, regulatory requirements, and clinical science objectives to effectively guide protocol design and strategy

  • Explore AI-based solutions and innovative technologies to optimize medical writing and editing workflows

Who You Are:

  • Eight or more years of medical writing and clinical project management experience, preferably in the biotech/pharmaceutical industry

  • Master's degree or PhD in a scientific or life sciences discipline or liberal arts preferred; or equivalent experience

  • Exceptional written and oral communication skills, with a proven ability to communicate effectively with stakeholders across the organization

  • Strong project management and team facilitation skills, including the ability to navigate conflicting opinions and build consensus under pressure

  • Expertise in clinical, scientific, and/or regulatory writing, with experience leading authoring, review, and finalization of complex documents

  • Strong analytical, planning, and organizational skills, with experience prioritizing high-volume workflows, managing simultaneous projects to completion, and ensuring the highest level of accuracy under tight deadlines

  • Commitment to collaborative and customer-focused work, demonstrating strong interpersonal skills and the ability to form effective working relationships in a complex, fast-paced environment

Onsite presence on our South San Francisco campus is expected for at least 3 days a week.

Relocation benefits are not available for this job posting.

The expected salary range for this position based on the primary location of California is $113,800 - $211,400. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

Benefits

#LI-JD1

#ECD

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

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About Genentech

Sourced by ZipRecruiter

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

South San Francisco, CA, US

Year founded

1976

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