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Writing Director Jobs in California (NOW HIRING)

INTELLISWIFT INC

Frontend Web Developer

San Jose, CA · On-site

Candidate should have strong experience on writing direct javascript without using libraries. Experience with cross-browser, cross-platform, and design constraints on the web. Experience in software ...

Abbott

Head of Copy

Alameda, CA · On-site

Write, direct, and elevate copy across all touchpoints - brand, digital, editorial, CRM, and beyond * Set the standard for what great writing looks like at Lingo, providing hands-on guidance and ...

Jobsbridge

Frontend Web Developer

San Jose, CA

Candidate should have strong experience on writing direct javascript without using libraries. Experience with cross-browser, cross-platform, and design constraints on the web. Experience in software ...

Abbott

Head of Copy

Alameda, CA

Write, direct, and elevate copy across all touchpoints - brand, digital, editorial, CRM, and beyond * Set the standard for what great writing looks like at Lingo, providing hands-on guidance and ...

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Writing Director information

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How much do writing director jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for writing director in California is $33.97, according to ZipRecruiter salary data. Most workers in this role earn between $16.95 and $39.08 per hour, depending on experience, location, and employer.

What skills and qualifications are needed to be a writing director?

To thrive as a Writing Director, you need advanced writing and editing skills, a strong command of language and storytelling, and typically a bachelor's degree in English, journalism, or a related field. Familiarity with content management systems (CMS), project management tools, and editing software is commonly required. Leadership, creative vision, and the ability to mentor and collaborate with writers are essential soft skills. These competencies ensure high-quality content, cohesive team performance, and effective communication of brand or organizational messages.

How to become a writing director?

To become a writing director, candidates typically need extensive experience in writing and editing, often starting in entry-level writing or editing roles. Developing strong leadership, project management skills, and a deep understanding of storytelling or content creation are essential, along with a portfolio demonstrating successful projects. Many writing directors also hold relevant degrees or certifications in writing, communications, or related fields.

What is the difference between Writing Director vs Content Manager?

AspectWriting DirectorContent Manager
CredentialsTypically requires a degree in English, Journalism, or related fields; extensive writing and leadership experienceOften requires a degree in Marketing, Communications, or related fields; experience in content strategy and management
Work EnvironmentCreative agencies, publishing houses, media companies, corporate communicationsDigital marketing firms, media companies, corporate websites, social media teams
Industry UsageUsed in organizations focusing on content creation, storytelling, and editorial directionUsed in organizations managing content production, distribution, and strategy

The main difference is that a Writing Director oversees the overall writing and editorial vision, focusing on high-level content strategy and leadership. In contrast, a Content Manager handles day-to-day content operations, scheduling, and distribution. Both roles require strong writing skills, but the Writing Director is more strategic and creative, while the Content Manager is more operational and tactical.

What is a writing director?

A Writing Director is a professional responsible for overseeing and guiding the writing process within an organization or production. They lead a team of writers, set the tone and style for written content, and ensure that all materials align with the project's objectives and standards. Writing Directors often work in fields such as film, television, publishing, or marketing, providing editorial direction, managing deadlines, and collaborating with other creative departments to deliver cohesive and high-quality content.

How does a writing director typically collaborate with other departments within an organization?

A Writing Director often works closely with teams such as marketing, design, product, and communications to ensure consistency and alignment in messaging across all platforms. They provide strategic direction, review content, and coordinate with stakeholders to meet organizational goals. This role frequently involves leading brainstorming sessions, setting editorial standards, and managing feedback to refine the overall voice and tone of the company. Effective collaboration is key to maintaining a unified brand narrative and achieving project milestones.

What are the most commonly searched types of Writing jobs in California?

The most popular types of Writing jobs in California are:

What are popular job titles related to Writing Director jobs in California?

For Writing Director jobs in California, the most frequently searched job titles are:

What job categories do people searching Writing Director jobs in California look for?

The top searched job categories for Writing Director jobs in California are:

What cities in California are hiring for Writing Director jobs?

Cities in California with the most Writing Director job openings:

Writing Director jobs near you
Infographic showing various Writing Director job openings in California as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 2% Temporary, and 1% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $70,656 per year, or $34 per hour.

Associate Director, Regulatory and Medical Writer

Ionis

Carlsbad, CA • On-site, Remote

Full-time

Re-posted 26 days ago

Job description

Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland, Ionis has been at work for more than three decades discovering medical breakthroughs that have redefined life for people with serious diseases. We're pioneers in RNA-targeted medicines, and our platform continues to revolutionize drug discovery and transform lives for patients with unmet needs. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.
At Ionis, we pride ourselves on cultivating a challenging, motivating and rewarding environment that fosters innovation and scientific excellence. We know that our success is a direct result of the exceptional talents and dedication of our employees.
With an unprecedented opportunity to change the course of human health, we look to add diverse individuals, skill sets and perspectives to our exceptional team. We continue to invest time, money and energy into making our onsite, hybrid and remote work environments a place where solid and lasting relationships are built and where our culture and employees can thrive.
We're building on our rich history, and we believe our greatest achievements are ahead of us. If you're passionate about the opportunity to have meaningful impact on patients in need, we invite you to apply and join us. Experience and contribute to our unique culture while you develop and expand your career!
ASSOCIATE DIRECTOR - REGULATORY AND MEDICAL WRITING
SUMMARY:
The Associate Director, Medical Writing is responsible for leading the planning, development, and delivery of complex clinical and regulatory documents in support of global regulatory submissions and development programs.
This role provides strategic leadership within the Regulatory and Medical Writing function, serving as a key partner to Clinical Development, Biostatistics, and other cross-functional teams to ensure high-quality, scientifically rigorous, and compliant regulatory documentation.
The Associate Director will lead medical writing activities across multiple programs, drive document strategy and messaging, and contribute to regulatory submission planning. This position may also mentor and guide other medical writers while ensuring consistency, quality, and adherence to regulatory standards.
This role reports to the Executive Director (Head) of Regulatory and Medical Writing.
This position may be fully remote; however, preference will be given to San Diego-based applicants.
RESPONSIBILITIES:
  • Working with the Executive Director, Regulatory and Medical Writing, lead the development, authoring, and delivery of complex regulatory documents such as clinical study reports and marketing application summary documents (Module 2), and lead and/or contribute to Investigator's Brochures, clinical study protocols, and briefing documents.
  • Serve as Regulatory Medical Writing lead on cross-functional program teams, partnering with Clinical Development, Regulatory Affairs, Biostatistics, Safety, and other stakeholders.
  • Provide strategic input into regulatory document planning and submission strategies to support global regulatory filings.
  • Serve as Medical Writing department lead on multiple project/core teams.
  • Function as subject matter expert within the department for assigned therapeutic/product areas.
  • Responsible for planning (in collaboration with Global Project Management) and leading cross-functional teams to meet timelines for deliverables.
  • Lead complex scientific key messaging/storyboarding cross-functional meetings, ensuring the messages are clear and consistent within and across documents.
  • Understand, assimilate, and interpret sources of information independently.
  • Ensure compliance with appropriate conventions, proper grammar usage, and correct format requirements, as needed (e.g., formatting, hyperlinking).
  • Manage review cycles for documents; schedule and lead data interpretation meetings, comment resolution meetings, and other document-related meetings.
  • Perform quality control (QC) reviews as necessary.
  • Interact with Quality Assurance (QA) as document lead to resolve audit findings for specific documents.
  • Maintain expert knowledge of US and international regulations, requirements, and guidance associated with preparation of regulatory documentation.
  • Effectively coordinate with Regulatory Operations to ensure on-time preparation and publication of regulatory submission documents.
  • Support Global Regulatory Lead with preparing information/responses requested by regulatory agencies.
  • Mentor and provide guidance to junior and senior medical writers, contributing to departmental best practices and writing standards.
  • Other duties as assigned.

REQUIREMENTS:
  • Bachelor's degree required; advanced degree in a scientific, clinical, or regulatory field preferred.
  • 12+ years of medical writing experience in the pharmaceutical industry, including marketing applications (e.g., Module 2.5, 2.7.3, 2.7.4). Rare disease experience a plus.
  • Proven lead writer experience for key regulatory documents (e.g., CSRs, protocols, IBs, INDs, NDAs, briefing documents), strong expertise in safety sections preferred.
  • Demonstrated experience leading medical writing activities for major regulatory submissions, including marketing applications.
  • Significant experience as lead writer for Module 2 summary documents (e.g., 2.5, 2.7.1, 2.7.2, 2.7.3, and 2.7.4) and other key regulatory documents.
  • Experience writing clinical study reports, Investigator Brochures, clinical protocols, IND/NDA sections, and regulatory briefing documents. In depth experience writing Safety sections of regulatory documents preferred.
  • Experience writing requests for regulatory designations (e.g., Breakthrough Designation, Orphan Drug, Sakigake, PRIME, etc) a plus.
  • Strong understanding of the drug development lifecycle and regulatory submission processes.
  • Extensive knowledge of FDA, EMA, and ICH guidelines (especially ICH E3 and E6[R3]).
  • Demonstrated ability to lead cross-functional teams and manage complex document development projects.
  • Strong ability to interpret complex scientific and clinical data and translate it into clear regulatory narratives.
  • Proficiency in American Meical Association (AMA) style guidelines.
  • Advanced attention to detail with expertise in scientific editing, formatting, and document QC.
  • Technical proficiency with Microsoft Office and Adobe Acrobat, and document management systems such as Veeva.
  • Experience with StartingPoint templates preferred.
  • Advanced written and verbal communication skills (including presentations), and project management skills, with the ability to clearly communicate complex scientific concepts across functional teams.
  • Extensive experience using style guides, lexicons, and eCTD requirements.
  • Demonstrated ability to mentor writers and contribute to a collaborative team environment.
  • Energetic, self-motivated, and able to thrive in a dynamic, intense, and fast-paced environment.
  • Strong team orientation with the ability to lead initiatives and drive results across cross-functional teams.
  • Advanced time-management skills. Ability to balance multiple projects simultaneously.

A brief medical writing exercise may be requested prior to interview.
Please visit our website, http://www.ionis.com for more information about Ionis and to apply for this position; reference requisition # IONIS003873
Ionis offers an excellent benefits package! Follow this link for more details: Ionis Benefits
Full Benefits Link: https://www.ionis.com/careers/working-at-ionis/#:~:text=our%20employee%20spotlight-,Benefits,-Employees%20are%20rewarded
The pay scale for this position is $142,588 to $201,472
NO PHONE CALLS PLEASE. PRINCIPALS ONLY.
Ionis Pharmaceuticals, Inc. and all its subsidiaries are proud to be EEO employers.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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