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Script Writing Jobs in Oakland, CA (NOW HIRING)

ClifyX

ServiceNow Admin

San Ramon, CA · On-site

Basic understanding and ability to script automated processes. AgileScrum methodology experience ... Good oral and written communication skills. Strong analytical, teamwork and customer engagement ...

Sonatus

Hardware Prototyping & Lab Lead

Sunnyvale, CA · On-site

Bridge the gap between hardware, software, and QA by writing scripts and tools that connect lab equipment, test automation, and engineering workflows. * Lead Lab Innovation: Take full ownership of ...

Jobsbridge

Lead Hadoop Developer

San Jose, CA

... HDFS writing sqoop scripts, pig and mapreduce jobs, and designing hive queries. Must be having team handling experience Skilled with star join schema design and development processes required ...

Jobsbridge

QA Engineer - Automation

Fremont, CA

Write test cases and execute test scripts, edit and maintain existing test scripts working with product managers and engineering teams to document defects. Identify issues within scope and schedule ...

Cisco

Content Writer (Remote)

San Francisco, CA · On-site +1

$165K - $210K/yr

Write and edit content across multiple formats, including video scripts, blog posts, social media copy, executive talking points, presentations, and internal/external communications * Maintain and ...

Cisco

Content Writer (Remote)

San Jose, CA · On-site +1

$165K - $210K/yr

Write and edit content across multiple formats, including video scripts, blog posts, social media copy, executive talking points, presentations, and internal/external communications * Maintain and ...

Audacy, Inc.

News Writer (Part-Time)

San Francisco, CA

$22.02 - $38.02/hr

... scripts for news anchors to deliver via radio broadcast and digital stream * Write compelling ... Edit and produce newscasts (including but not limited to selecting, editing and/or writing news ...

Audacy, Inc.

News Writer (Part-Time)

San Francisco, CA · On-site

$22.02 - $38.02/hr

... scripts for news anchors to deliver via radio broadcast and digital stream * Write compelling ... Edit and produce newscasts (including but not limited to selecting, editing and/or writing news ...

Cisco

Content Writer (Remote)

San Jose, CA · On-site +1

$165K - $210K/yr

Write and edit content across multiple formats, including video scripts, blog posts, social media copy, executive talking points, presentations, and internal/external communications * Maintain and ...

Audacy, Inc.

News Writer (Part-Time)

San Francisco, CA · On-site

$22.02 - $38.02/hr

... scripts for news anchors to deliver via radio broadcast and digital stream * Write compelling ... Edit and produce newscasts (including but not limited to selecting, editing and/or writing news ...

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All JobsScript Writing JobsScript Writing Jobs in Oakland, CA

Script Writing information

See Oakland, CA salary details

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How much do script writing jobs pay per year?

As of Aug 9, 2026, the average yearly pay for script writing in Oakland, CA is $227,998.00, according to ZipRecruiter salary data. Most workers in this role earn between $208,200.00 and $247,800.00 per year, depending on experience, location, and employer.

Are script writers in demand?

Script writers are in demand in industries such as film, television, and digital media, especially as content creation continues to grow. Strong storytelling skills, familiarity with industry-standard software, and the ability to adapt to different genres increase employability in this field.

How do script writers typically collaborate with directors and producers during a project?

Script writers often work closely with directors and producers throughout the development and production process. After submitting a draft, writers may participate in meetings to discuss revisions based on creative direction, budget, or logistical constraints. Open communication and flexibility are essential, as scripts frequently evolve to align with the director's vision and production needs. This collaboration ensures the final script serves the story while being feasible to produce, offering writers valuable insights and professional growth.

How much do script writers get paid?

Script writers' salaries vary based on experience, industry, and project type. Entry-level writers typically earn between $30,000 and $60,000 annually, while experienced professionals can earn over $100,000 or more, especially in television and film. Freelance script writers may charge per project or per hour, depending on their reputation and the scope of work.

What is script writing?

Script writing is the process of creating written works that outline the dialogue, actions, and directions for productions such as films, television shows, plays, or video content. Script writers develop the story structure, characters, and settings, ensuring that the script conveys the intended message and emotions. This process often involves multiple drafts, collaboration with directors and producers, and adherence to specific formatting guidelines. Script writing is crucial for guiding actors and production teams in bringing a story to life.

What is the difference between Script Writing vs Screenwriting?

AspectScript WritingScreenwriting
CredentialsOften requires writing skills, storytelling, and sometimes film or media coursesTypically requires a degree in film, screenwriting, or related fields
Work EnvironmentCollaborative, creative settings such as production companies, advertising agencies, or media studiosFilm and television production environments, studios, or freelance
Industry UsageUsed across advertising, video games, theater, and media projectsPrimarily in film, television, and digital media

Script Writing is a broad term encompassing various types of scripts for different media, focusing on storytelling and dialogue. Screenwriting specifically refers to writing scripts for films and TV shows, often requiring industry-specific knowledge and formal training. While both roles involve storytelling and script development, screenwriters typically work within the film and television industry, whereas script writers may work across multiple media platforms.

Do script writers make money?

Script writers can earn varying incomes depending on their experience, the industry, and the type of projects they work on. Entry-level writers may earn less, while experienced professionals working on major films, TV shows, or with established agencies can make a substantial income. Many script writers supplement their income through multiple projects or freelance work.

What are the key skills and qualifications needed to thrive as a script writer, and why are they important?

To thrive as a Script Writer, you need strong storytelling abilities, mastery of script formatting, and a solid grasp of narrative structure, often supported by a degree in film, creative writing, or a related field. Familiarity with industry-standard software such as Final Draft or Celtx is typically required. Creativity, adaptability, and the ability to collaborate and accept feedback are crucial soft skills in this role. These competencies ensure compelling, well-structured scripts that meet industry standards and resonate with audiences.

What are script writing jobs?

Script writing jobs focus on creating general written content for the production of a video. This could take the form of a screenplay, copywriting for an advertisement, or even content for a video game. As a script writer, your job is to help deliver the story that your client wants to tell. To accomplish this, you decide the best way to deliver the content, create a storyboard to pitch the idea, and then write the actual script. Script writers are often given a lot of freedom when creating content, so creativity is crucial to your success. Script writing jobs also take place in a deadline-driven environment, so the ability to finish your work on time is essential.

More about Script Writing jobs
What are the most commonly searched types of Script Writing jobs in Oakland, CA? The most popular types of Script Writing jobs in Oakland, CA are:
What are popular job titles related to Script Writing jobs in Oakland, CA? For Script Writing jobs in Oakland, CA, the most frequently searched job titles are:
What job categories do people searching Script Writing jobs in Oakland, CA look for? The top searched job categories for Script Writing jobs in Oakland, CA are:
What cities near Oakland, CA are hiring for Script Writing jobs? Cities near Oakland, CA with the most Script Writing job openings:
Script Writing jobs near you
Infographic showing various Script Writing job openings in Oakland, CA as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 69% Full Time, 25% Part Time, 2% Temporary, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $227,998 per year, or $109.6 per hour.

Sr. Director, Head of Regulatory & Medical Writing

Nurix

Brisbane, CA • On-site

Full-time

Re-posted yesterday

Job description

Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix's dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
Job Summary:
As a key member of the cross-functional Development Team responsible for providing regulatory writing expertise and leadership to formulate the writing strategy for key regulatory documents for submission. The Sr. Director, Head of Regulatory & Medical Writing will be responsible for providing guidance to the medical and or regulatory writing group (contractors and internal writers) assigned to deliverables and ensuring appropriate work allocation and document preparation.; will also provide review and substantive editing of documents to ensure delivery of high-quality documents. This individual will work effectively with many other functional groups, including with Clinical Scientist(s), Medical Monitors, Regulatory and other functions as applicable, and collaborate with clinical medical writing as applicable to ensure scientific excellence in the execution of clinical trials. The Head of Regulatory Writing will build a medical writing group internally when appropriate.
Reporting to the SVP, Head of Regulatory Affairs, this role will be responsible for the regulatory writing & medical writing deliverables of assigned project(s), in accordance with the agreed timelines and quality standards.
Responsibilities:
  • Ensure appropriate allocation of internal and external resources needed for all regulatory writing deliverables.
  • Hire and manage medical writers internally and manage external medical writing contractors.
  • Forecasting and maintaining budget for the regulatory writing team.
  • Assess efficiencies, help identify areas of improvement and initiate improvement processes.
  • Coordinate, author and edit documents used to support clinical trial conduct and reporting including but not limited to:
    • Clinical study protocols and clinical protocol amendments (in partnership with Clinical Science/Clinical Development)
    • Clinical study reports
    • Investigator's brochures and annual updates
    • IND submissions and annual reports
    • Lay-person summary
    • Integrated summary reports
    • Clinical, Nonclinical and Multidisciplinary Information Amendments
    • NDA, BLA, MAA, (e)CTD submissions
    • Risk Management Plans
    • Health Authority responses
    • Briefing Documents, ODDs, BTDs/PRIME, FTD etc
  • Participate in relevant subteam(s) and ensure effective planning and management of timelines for all components of assigned documents across all projects.
  • Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects.
  • Support and develop deliverables required for global transparency and disclosure requirements (e.g., plain language lay summary, applicable redactions to regulatory documents subject to EU posting regulations and results for EU CTR).Partner with Biometrics in developing standard TFLs and in text tables for deliverables as applicable
  • Maintain and support developing and reviewing standard processes and templates.
  • Review and edit documents as required.
  • Work effectively and lead in cross-functional working groups.

Qualifications:
  • Candidates must have a BS with 15+ years, or MS or other advanced science degree (e.g.: RN, NP, MSN, PharmD, PhD, MD) with 10+ years of experience in oncology clinical research experience as a clinical or regulatory medical writer within the pharmaceutical/biotech industry.
  • Prior experience leading a regulatory writing group
  • Experience writing/leading the writing of critical clinical documents in major regulatory filings (NDA, BLA, MAA).
  • Proficiency in the use and understanding of computer software e.g. word processing, graphics, reference manager, document management systems.
  • Familiarity with all phases of drug development processes (discovery to market), clinical study protocol design, CTA/IND submissions, investigator's brochures and clinical study data collection and results reporting.
  • Advanced knowledge of routine document content preparation, including the use of style guides, medical dictionaries, and regulatory guidance documents and templates.
  • Experience writing, at a minimum, protocols (Phase 1-3, in oncology), investigator's brochures, clinical study reports, Health Authority briefing packages, and Health Authority responses. Experience with Pediatric Investigational Plans (PIPs) is preferred.
  • Advanced understanding/knowledge of regulatory requirements and drug development processes, Good Clinical Practice (GCP), regulatory requirements and guidelines associated with regulatory documents (e.g., protocols, investigator brochures, and clinical study reports).
  • Ability to interpret and summarize complex tabular and graphical data presentations.
  • Strong organization, documentation and communication skills with an ability to multitask.
  • Adaptable / flexible, willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism.
  • Detailed knowledge of GCP, ICH Guidelines and current US FDA regulations.

Salary Range: $254,127 - $289,388 plus bonus and equity.
Nurix Therapeutics, Inc. is committed to protecting and respecting your privacy and personal information, including information collected by Nurix when you apply for a job with Nurix or in the course of your employment with Nurix. By applying for a position at Nurix, you agree to our collection and use of personal information as described in our Privacy Policy (https://www.nurixtx.com/privacy-policy/).

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