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BeiGene, Inc.

Principal Medical Writer

Document Writing: * Manages the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as BeiGene SOP/WI(s), template(s), and style guide. * Be able ...

Veristat

The Principal Medical Writer independently plans and prepares a range of regulatory documents and/or medical communications to support all phases of product development. The primary responsibilities ...

New

Merck Group

Senior Principal Medical Writer

Billerica, MA · On-site

$126K - $215K/yr

As the Senior Principal Medical Writer, you will lead the end-to-end development of complex regulatory submission documents - ensuring high communication quality, scientific rigor, regulatory ...

Veristat

The Principal Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary responsibilities of ...

New

Collier County Public Schools

Principal Pool

Naples, FL · On-site

Administrative/Principal Date Posted: 4/13/2026 Location: Multiple Locations Date Available: 2026 ... Writing Sample (questions embedded in application can be uploaded to the application as a PDF form ...

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Principal Writer information

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$11K

$186.5K

How much do principal writer jobs pay per year?

As of Jul 16, 2026, the average yearly pay for principal writer in the United States is $185,359.00, according to ZipRecruiter salary data. Most workers in this role earn between $185,000.00 and $185,500.00 per year, depending on experience, location, and employer.

How does a Principal Writer typically collaborate with subject matter experts and other team members on complex projects?

Principal Writers often serve as key liaisons between subject matter experts (SMEs), editors, and project managers, ensuring that technical or specialized content is accurately translated for the intended audience. They frequently lead content development meetings, coordinate feedback from various stakeholders, and mentor junior writers on best practices. Effective collaboration requires strong communication skills, adaptability, and the ability to synthesize input from multiple sources while maintaining consistency and clarity in the final deliverables.

What is a Principal Writer?

A Principal Writer is a senior-level professional responsible for creating, managing, and overseeing high-quality written content, often in specialized fields such as technical writing, medical communications, or corporate communications. They serve as subject matter experts, provide strategic guidance on content development, and may mentor or supervise other writers. Principal Writers ensure that documentation or publications meet organizational standards and are clear, accurate, and effective for their intended audiences.

What is the difference between Principal Writer vs Senior Writer?

AspectPrincipal WriterSenior Writer
CredentialsBachelor's degree in English, Communications, or related field; extensive writing experienceBachelor's degree; several years of professional writing experience
Work EnvironmentLead role in content strategy, overseeing multiple projects and teamsFocus on producing high-quality content, often mentoring junior writers
Employer & Industry UsageUsed in corporate, publishing, and media companies for senior content leadershipCommon in marketing, publishing, and media industries for experienced writers

The Principal Writer typically holds a higher level of responsibility, overseeing content strategy and managing teams, whereas the Senior Writer focuses on creating and refining content with less managerial duties. Both roles require strong writing skills and relevant experience, but the Principal Writer often leads projects and sets content direction.

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

To thrive as a Principal Writer, you need advanced writing and editing expertise, a deep understanding of subject matter, and often a relevant degree in English, communications, or a specialized field. Familiarity with content management systems, document collaboration tools, and style guides like AP or Chicago Manual of Style is typically required. Exceptional communication, leadership, and project management skills help distinguish top performers in this senior role. These abilities ensure the production of high-quality, consistent content and effective guidance of writing teams or projects.
More about Principal Writer jobs
What job categories do people searching Principal Writer jobs look for? The top searched job categories for Principal Writer jobs are:
Principal Writer jobs near you
Infographic showing various Principal Writer job openings in the United States as of July 2026, with employment types broken down into 89% Full Time, 9% Part Time, 1% Temporary, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $185,359 per year, or $89.1 per hour.
Principal Medical Writer

Principal Medical Writer

BeiGene, Inc.

Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 16 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
This position is responsible for providing expertise to support the development of high-quality, fit-for-purpose clinical and regulatory documents to facilitate speed of information during development, submission, approval, and life-cycle management of products in BeiGene pipeline. The clinical and regulatory documents include, but are not limited to, clinical study protocols, investigator brochures, clinical study reports, regulatory briefing documents, clinical modules of INDs, NDAs, BLAs, MAAs and other regulatory submissions, and other types of clinical and regulatory documents within the working scope of global medical writing. This position is also responsible for mentoring MWs (full-time employees and/or contractors/vendors) as needed.
Essential Functions of the Job:
Document Writing:
  • Manages the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as BeiGene SOP/WI(s), template(s), and style guide.

  • Be able to manage multiple documents at the same time, including the complex documents (eg, those with complex content, urgent timeline, or external collaboration). Proactively leads direction and strategy setting (including critically analyzing, synthesizing, and presenting complex information) for document development in collaboration with study team(s), and be able to guide other MWs.

  • Leads part of the creation of document writing template/guidance for all document types within the working scope. Leads the maintenance of document writing template/guidance for all document types within the working scope.

Project /Program Management:
  • Navigates through uncertainties to develop and manage timeline of individual documents and multiple documents (supported by different MWs in one project, eg, works as the MW filing lead for an NDA/BLA/MAA submission), including those for complex projects. Be able to guide other MWs.

  • Proactively identifies the questions/issues/potential risks that require departmental discussion or team discussion. Proactively identifies the potential risks and makes a mitigation plan. Resolves problems efficiently and skillfully. Be able to guide other MWs in these areas.

  • Builds strong and in-depth relationship with study team(s) and program team(s) (eg, works as the MW program lead).

  • Understands the role of own documents within the larger dossier and voices out any impact on upstream and downstream processes. Be able to guide other MWs and provide suggestions.

Process/Tool Establishment and Optimization:
  • Proactively identifies needs for process/tool optimization and establishment, and proposes solutions.

  • Leads departmental process/tool optimization. Leads (part of) departmental process/tool establishment.

  • Leads part of cross-functional process/tool optimization. Contributes to cross-function process/tool establishment.

  • Contributes to cross-company process/tool optimization.

Training and Mentoring:
  • Leads (part of) the development of new training programs. Provides instructions/trainings (content-wise/process-wise) to other MWs.

  • Provides systematic technical and operational mentorship to MWs (full-time employees and/or contractors/vendors).

Influence:
  • Understands the global MW scope and works to guide study team(s) and program team(s) within the defined scope and responsibility following established processes.

  • Provides topic sharing on regulatory writing and related knowledge within the department and to cross-functional stakeholders.

  • Provides topic sharing on regulatory writing and related knowledge across companies (eg, meetings of DIA and medical writing communities).

Supervisory Responsibilities:
  • None.

Education Required:
  • An advanced degree (MS/PhD/PharmD/MD) in life science, pharmacy, medical, or health-related science is preferred.

  • BS with a minimum of 5+ years of regulatory document writing (or equivalent) experience, Masters with 4+ or PhD/PharmD/MD with a minimum of 2+ years of regulatory document writing (or equivalent) experience.

Computer Skills:
Technical expertise in Microsoft Word, Adobe Acrobat, and electronic document management systems; proficiency in Microsoft Outlook, Excel, and PowerPoint, etc.
Travel:
On occasion, as needed.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $119,300.00 - $159,300.00 annually
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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