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Medical Script Jobs in California (NOW HIRING)

Residents Medical

Director of Sales

Los Angeles, CA

Design and refine the sales process, scripts, and CRM workflow; report on conversion metrics and revenue forecasts to leadership. * Develop partnerships and referral channels (international medical ...

Residents Medical

Director of Sales

Los Angeles, CA · On-site

Design and refine the sales process, scripts, and CRM workflow; report on conversion metrics and revenue forecasts to leadership. * Develop partnerships and referral channels (international medical ...

Residents Medical

Director of Sales

Los Angeles, CA · On-site

Design and refine the sales process, scripts, and CRM workflow; report on conversion metrics and revenue forecasts to leadership. * Develop partnerships and referral channels (international medical ...

Kitu Systems

Software Test Engineer

San Diego, CA

... test cases, scripts, and tools to implement test plans Develop scripts and tools to automate ... that includes Medical, Dental, Vision, and Life Coverage in addition to PTO. The position is ...

Kitu Systems

Software Test Engineer

San Diego, CA · On-site

... scripts, and tools to implement test plans • Develop scripts and tools to automate testing • ... that includes Medical, Dental, Vision, and Life Coverage in addition to PTO. The position is ...

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Medical Script information

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How much do medical script jobs pay per hour?

As of Jul 22, 2026, the average hourly pay for medical script in California is $20.27, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $22.55 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Medical Script position, and why are they important?

As a Medical Scribe, you need a strong understanding of medical terminology, attention to detail, and fast, accurate typing skills, typically supported by relevant coursework or healthcare experience. Familiarity with electronic health record (EHR) systems and, in some cases, scribe certification is highly valued. Excellent listening, communication, and time management skills help you collaborate effectively with physicians and healthcare staff. These abilities are essential for creating precise documentation that supports high-quality patient care and smooth clinical operations.

What is a Medical Script job?

A Medical Script job typically involves writing or reviewing medical documents, such as prescriptions, treatment plans, or healthcare-related scripts for media and patient education. Professionals in this role require knowledge of medical terminology and compliance with healthcare regulations. They may work in hospitals, clinics, pharmaceutical companies, or media agencies to ensure accuracy and clarity in medical communication.

What does a typical workday look like for a Medical Scribe?

A typical workday as a Medical Scribe involves accompanying physicians during patient visits, either in-person or remotely, and documenting clinical encounters in real time using electronic health record (EHR) systems. You will capture detailed notes on patient history, physical exams, and treatment plans, ensuring that all documentation is accurate and complete before the physician finalizes it. Scribes also help manage clinical workflows by tracking lab results, orders, and patient follow-ups. You'll work closely with medical teams in a fast-paced environment, gaining valuable firsthand experience in healthcare settings that can be beneficial for future career growth.

What are popular job titles related to Medical Script jobs in California? For Medical Script jobs in California, the most frequently searched job titles are:
What job categories do people searching Medical Script jobs in California look for? The top searched job categories for Medical Script jobs in California are:
What cities in California are hiring for Medical Script jobs? Cities in California with the most Medical Script job openings:
Medical Script jobs near you
Infographic showing various Medical Script job openings in California as of July 2026, with employment types broken down into 1% As Needed, 78% Full Time, 14% Part Time, and 7% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $42,162 per year, or $20.3 per hour.

Sr. Director, Head of Regulatory & Medical Writing

Nurix

Brisbane, CA • On-site

Full-time

Posted 14 days ago

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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