Clinical Documentation Lead
$113K - $211K/yr
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 ...
$113K - $211K/yr
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 ...
$113K - $211K/yr
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 ...
South San Francisco, CA · On-site
$113.80 - $211.40/hr
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 ...
South San Francisco, CA · On-site
$113.80 - $211.40/hr
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 ...
South San Francisco, CA · On-site
$113K - $211K/yr
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 ...
South San Francisco, CA · On-site
$113K - $211K/yr
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 ...
The Commissioning & Qualification (C&Q) Documentation Lead is responsible for developing, authoring, and managing commissioning and qualification documentation in support of GMP-regulated projects.
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The Commissioning & Qualification (C&Q) Documentation Lead is responsible for developing, authoring, and managing commissioning and qualification documentation in support of GMP-regulated projects.
Arlington, TX · On-site
$24/hr
Takes a lead role in creating and maintaining documents used internally and managed by the Quality Management System (QMS) * Assists others in the interpretation of specifications and maintains ...
Arlington, TX · On-site
$24/hr
Takes a lead role in creating and maintaining documents used internally and managed by the Quality Management System (QMS) * Assists others in the interpretation of specifications and maintains ...
New Haven, CT · On-site
$35 - $47/hr
The HCC Documentation Lead will serve as a partner and subject matter expert on HCC coding and documentation for clinicians who are a part of our Clinically Integrated Network (CIN), Yale New Haven ...
New Haven, CT · On-site
$35 - $47/hr
The HCC Documentation Lead will serve as a partner and subject matter expert on HCC coding and documentation for clinicians who are a part of our Clinically Integrated Network (CIN), Yale New Haven ...
New Haven, CT · On-site
$35 - $47/hr
The HCC Documentation Lead will serve as a partner and subject matter expert on HCC coding and documentation for clinicians who are a part of our Clinically Integrated Network (CIN), Yale New Haven ...
New Haven, CT · On-site
$35 - $47/hr
The HCC Documentation Lead will serve as a partner and subject matter expert on HCC coding and documentation for clinicians who are a part of our Clinically Integrated Network (CIN), Yale New Haven ...
New Haven, CT · On-site
$35 - $47/hr
The HCC Documentation Lead will serve as a partner and subject matter expert on HCC coding and documentation for clinicians who are a part of our Clinically Integrated Network (CIN), Yale New Haven ...
New Haven, CT · On-site
$35 - $47/hr
The HCC Documentation Lead will serve as a partner and subject matter expert on HCC coding and documentation for clinicians who are a part of our Clinically Integrated Network (CIN), Yale New Haven ...
Fort George G Meade, MD · On-site
$95K - $115K/yr
Act as a documentation lead, working closely with software engineers, project managers, and stakeholders to ensure documentation aligns with project milestones and Agile sprints. * Compliance & A&A ...
Fort George G Meade, MD · On-site
$95K - $115K/yr
Act as a documentation lead, working closely with software engineers, project managers, and stakeholders to ensure documentation aligns with project milestones and Agile sprints. * Compliance & A&A ...
Baltimore, MD · On-site +1
$34.50 - $46.50/hr
Lead Improvement Initiatives: Drive efforts to enhance clinical documentation and coding quality through strategic recommendations and collaboration. * Leverage EMR Software: Document clarification ...
Baltimore, MD · On-site +1
$34.50 - $46.50/hr
Lead Improvement Initiatives: Drive efforts to enhance clinical documentation and coding quality through strategic recommendations and collaboration. * Leverage EMR Software: Document clarification ...
San Antonio, TX · On-site
... documentation Lead knowledge transfer sessions with technical and business stakeholders Present executive-level readouts, including roadmap recommendations and next-phase guidance Lead end-to-end ...
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San Antonio, TX · On-site
... documentation Lead knowledge transfer sessions with technical and business stakeholders Present executive-level readouts, including roadmap recommendations and next-phase guidance Lead end-to-end ...
Abilene, TX · On-site
Conduct quality inspections, testing, and documentation to ensure work meets industry standards and ... Lead and coordinate field crews while promoting a safe, quality-focused work environment.
Abilene, TX · On-site
Conduct quality inspections, testing, and documentation to ensure work meets industry standards and ... Lead and coordinate field crews while promoting a safe, quality-focused work environment.
Abilene, TX · On-site
$105K - $145K/yr
Conduct quality inspections, testing, and documentation to ensure work meets industry standards and ... Lead and coordinate field crews while promoting a safe, quality-focused work environment.
Quick apply
Abilene, TX · On-site
$105K - $145K/yr
Conduct quality inspections, testing, and documentation to ensure work meets industry standards and ... Lead and coordinate field crews while promoting a safe, quality-focused work environment.
Portland, OR · On-site
$18 - $24/hr
Capture Matterport scans for documentation * Lead small crews/teams through the project, making sure demo, drying, and equipment setup get done right * Help set and monitor equipment (air movers ...
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Portland, OR · On-site
$18 - $24/hr
Capture Matterport scans for documentation * Lead small crews/teams through the project, making sure demo, drying, and equipment setup get done right * Help set and monitor equipment (air movers ...
Lead documentation efforts on all aspects of facility engineering, construction and validation across our global presence. * Technical lead for electronic management of engineering lifecycle ...
Lead documentation efforts on all aspects of facility engineering, construction and validation across our global presence. * Technical lead for electronic management of engineering lifecycle ...
Washington, DC · On-site
$30 - $35/hr
Provide senior-level guidance for evaluation planning, quarterly reporting, and transition documentation. * Lead and participate in high-visibility communications with federal stakeholders. * Support ...
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Washington, DC · On-site
$30 - $35/hr
Provide senior-level guidance for evaluation planning, quarterly reporting, and transition documentation. * Lead and participate in high-visibility communications with federal stakeholders. * Support ...
$96K - $134K/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 ...
$96K - $134K/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 ...
Phoenix, AZ · On-site
$70 - $90/hr
Lead clinical documentation improvement initiatives focused on orthopedic and musculoskeletal specialties * Review provider documentation for completeness, specificity, medical necessity, and coding ...
Phoenix, AZ · On-site
$70 - $90/hr
Lead clinical documentation improvement initiatives focused on orthopedic and musculoskeletal specialties * Review provider documentation for completeness, specificity, medical necessity, and coding ...
Raritan, NJ · On-site
$105K - $138K/yr
Lead the package design development and assessment, and develop, write, gain cross-functional alignment, and route for approval package development documentation. * Lead packaging development ...
Raritan, NJ · On-site
$105K - $138K/yr
Lead the package design development and assessment, and develop, write, gain cross-functional alignment, and route for approval package development documentation. * Lead packaging development ...
ESSENTIAL FUNCTIONS • Lead clinical documentation improvement initiatives focused on orthopedic and musculoskeletal specialties • Review provider documentation for completeness, specificity ...
ESSENTIAL FUNCTIONS • Lead clinical documentation improvement initiatives focused on orthopedic and musculoskeletal specialties • Review provider documentation for completeness, specificity ...
$30K - $46K
5% of jobs
$46K - $62K
1% of jobs
$62K - $78K
2% of jobs
$78K - $94K
4% of jobs
$94K - $110K
9% of jobs
$115.2K is the 25th percentile. Wages below this are outliers.
$110K - $126K
11% of jobs
$126K - $142K
11% of jobs
The median wage is $156.9K / yr.
$142K - $158K
8% of jobs
$158K - $174K
4% of jobs
$174K - $190K
2% of jobs
$196.7K is the 75th percentile. Wages above this are outliers.
$190K - $206K
43% of jobs
$30K
$156.3K
$206K
| Aspect | Documentation Lead | Technical Writer |
|---|---|---|
| Credentials | Typically requires experience in technical communication, project management, and industry-specific knowledge | Usually requires a degree in technical communication, journalism, or related fields; certifications like STC are common |
| Work Environment | Leads teams, manages documentation projects, collaborates with multiple departments | Creates and edits technical content, often working independently or within a small team |
| Industry Usage | Used in large organizations, especially in tech, engineering, and manufacturing sectors | Common 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.
The top searched job categories for Documentation Lead jobs are:

$113K - $211K/yr
Full-time
Posted 28 days ago
8.8
Based on 22 frontline employees who took The Breakroom Quiz
11th of 86 rated pharmaceutical
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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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.
Scientific research and development services
10,000+ Employees
South San Francisco, CA, US
1976