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Senior Medical Writer Jobs in Riverside, CA (NOW HIRING)

Senior Medical Equipment Planner 2 | San Diego, CA IMEG is hiring a Senior Medical Equipment ... written communication to individuals or groups Proficient with MS Office Suite including but not ...

Senior Medical Equipment Planner 2 | San Diego, CA IMEG is hiring a Senior Medical Equipment ... written communication to individuals or groups Proficient with MS Office Suite including but not ...

AI is seeking a talented and detail-oriented Sr. Medical Lab Technician to join our team. At ... Effective communication skills in English, both verbal and written. * Must have exceptional ...

AI is seeking a talented and detail-oriented Sr. Medical Lab Technician to join our team. At ... Effective communication skills in English, both verbal and written. * Must have exceptional ...

AI is seeking a talented and detail-oriented Sr. Medical Lab Technician to join our team. At ... Effective communication skills in English, both verbal and written. * Must have exceptional ...

AI is seeking a talented and detail-oriented Sr. Medical Lab Technician to join our team. At ... Effective communication skills in English, both verbal and written. Must have exceptional ...

New

Associate Medical Director

Irvine, CA · On-site

$283K - $320K/yr

POSITION WITHIN THE ORGANIZATION 1. Reports to Senior Medical Director, Laboratory Services 2. ... writing with all levels of staff o Skill and ability to learn and collaborate with others in a ...

Technical Writer

Irvine, CA · On-site

$85K - $110K/yr

Minimum 3 years of experience in technical writing, prefer medical background. * Excellent ... Sr., Lead or Manager). The compensation range for these roles are $85,000 - $110,000. About Us ...

Technical Writer

Irvine, CA · On-site

$85K - $110K/yr

Minimum 3 years of experience in technical writing, prefer medical background. * Excellent ... Sr., Lead or Manager). The compensation range for these roles are $85,000 - $110,000. About Us ...

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Senior Medical Writer information

See Riverside, CA salary details

$36.5K

$143.2K

$258.2K

How much do senior medical writer jobs pay per year?

As of Aug 18, 2026, the average yearly pay for senior medical writer in Riverside, CA is $143,226.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,500.00 and $173,200.00 per year, depending on experience, location, and employer.

What is a senior medical writer?

A Senior Medical Writer is responsible for creating clear, accurate, and compliant medical documents, including regulatory submissions, clinical study reports, and scientific publications. They work closely with cross-functional teams, such as medical affairs, regulatory affairs, and clinical teams, to ensure high-quality content. Senior Medical Writers also review and edit documents for consistency, clarity, and adherence to industry guidelines. Often, they mentor junior writers and contribute to process improvements within the medical writing team.

What are the key skills and qualifications needed to thrive as a senior medical writer?

To thrive as a Senior Medical Writer, you need advanced writing and editing skills, a thorough understanding of scientific and medical concepts, and typically a degree in a life science or related field. Familiarity with referencing tools (like EndNote), document management systems, and compliance with regulatory guidelines (such as ICH or FDA standards) is often required. Strong attention to detail, project management abilities, and the capacity to communicate complex ideas clearly are important soft skills for this position. These competencies ensure accurate, high-quality medical content that meets industry standards and supports effective communication among healthcare professionals and stakeholders.

What are some common challenges faced by senior medical writers, and how can they be addressed?

Senior Medical Writers often encounter challenges such as managing tight deadlines, interpreting complex scientific data, and ensuring adherence to strict regulatory requirements. To navigate these challenges, it's essential to have strong organizational skills, effective communication with project teams, and a solid grasp of industry guidelines. Many Senior Medical Writers find that staying current with new regulations, participating in ongoing professional development, and leveraging collaborative tools help streamline the workflow. By proactively addressing these challenges, writers can maintain accuracy and efficiency while contributing valuable expertise to cross-functional teams.

What are the most commonly searched types of Medical Writer jobs in Riverside, CA?

The most popular types of Medical Writer jobs in Riverside, CA are:

What are popular job titles related to Senior Medical Writer jobs in Riverside, CA?

For Senior Medical Writer jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Senior Medical Writer jobs in Riverside, CA look for?

The top searched job categories for Senior Medical Writer jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Senior Medical Writer jobs?

Cities near Riverside, CA with the most Senior Medical Writer job openings:

Infographic showing various Senior Medical Writer job openings in Riverside, CA as of August 2026, with employment types broken down into 89% Full Time, 7% Part Time, and 4% Contract. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $143,226 per year, or $68.9 per hour.

Senior Medical Writer- Clinical Focus

Veristat

Ontario, CA • Remote

Full-time

Medical, Retirement

Posted 5 days ago


Job description

Job Description:

Overview

The Senior Medical Writer- Clinical Focus is a major contributor to document authorship for a variety of documents across different service lines. The Sr Medical Writer will be the project lead on smaller projects, interfacing directly with the client, but also support larger, more complex engagements as a member of a larger delivery team. Veristat is looking for individuals looking to use their expertise in clinical regulatory writing to lead teams and help clients achieve their goals.

Make an Impact at Veristat!

Join a global team with more than 30 years of expertise accelerating life-changing therapies to patients worldwide.

  • 105+ approved therapies for marketing applications prepared by Veristat
  • 480+ oncology projects in the past 5 years
  • 350+ rare disease projects delivered in the past 5 years
  • Flexible, inclusive culture - 70% remote workforce, 66% women-led teams Learn more about our core values here!

What we offer

The estimated hiring range for this role is $116K to 128K USD plus applicable bonus. This hiring range is specific to the US and will vary for other regions based upon local market data. Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.

Benefits vary by location and may include:

  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans

What we look for

Education, Experience, Training, and Knowledge:

  • Bachelor's degree
  • 3+ years of regulatory writing experience or equivalent experience with clinical related documentation
  • Understand regulatory authority guidelines and requirements to be able to lead an internal project team and anticipate the effects that writing practice conventions can have on the final product when seeking health authority approval/acceptance
  • Experience in the development of submission-level documents (does not require functioning as a document lead)
  • Experience in the development of clinical documents such as Clinical Study Reports, Investigator Brochures, protocols ISS and/or ISE

Skills & Abilities:

  • Intermediate proficiency with Microsoft Word skills (editing tools, creating and modifying tables and inserting figures) and document management techniques
  • Strong understanding of the document creation process and of the drug development lifecycle
  • Able to synthesize data across multiple data sources and documents to create summary reports
  • Ability to conduct/lead a CRM and successfully lead a project team to consensus
  • Ability to use logical arguments to persuade others when presenting ideas and suggestions, but also respond positively to opposing views voiced by others
  • Develops professional relationships with clients as a way to further the business relationship and maintain current industry knowledge
  • Ability to identify and institutionalize work practices that are most effective in order to ensure consistency in performance

Automated Decision Making: All applicants are reviewed by a member of the Veristat Talent Acquisition team; Veristat does not utilize an automated decision-making process.

Veristat is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.