Top 1418 Editor/Writer Jobs

Regulatory Writer and/or Regulatory QC/ Editor
Vir Biotechnology —Remote
- $90 - $120 an hour
- Remote
- 5 years
- Mid-level
- Analysis skills
Quick Apply
Technical Writer/Editor III
DirectViz Solutions, LLC —Remote
- Full-time
- Remote
- Microsoft Excel
- 5 years
- English
- Health insurance
- Paid time off
Quick Apply
Technical Writer/Editor
Artemis Arc —Remote
- Remote
- Microsoft Excel
- English
- Mid-level
15h
Technical Writer & Editor
Resource Innovations —California
- $85,000 - $115,000 a year
- Remote
- Microsoft Word
- Background check
- 5 years
- Commuter assistance
- Paid holidays
Quick Apply
Assistant Content Review Coordinator
FN Marketing —Remote
- $22 an hour
- Part-time
- Remote
- English
- Research
- Fair chance
- Flexible schedule
Quick Apply
1d
Copy Editor
Cognition Learning Group —Remote
- $142 - $213 a day
- Contract
- Remote
- English
- Mid-level
8d
Content Editor / Writer with Machine Learning Experience
AUQ —Remote
- Contract
- Mid-level
- AI
- Flexible schedule
Writer-Editor
US Immigration and Customs Enforcement —Washington, DC
- $143,913 - $187,093 a year
- Online Application
- Hybrid work
- Background check
- Psychiatry
- Customer service
- Paid holidays
- Loan repayment program
9d
Writer/Editor Disney Theme Parks Content
Cambrick Yard —Remote
- Email
- Mid-level
- Organizational skills
- Time management
Senior Technical Writer / Editor
Essential Healthcare Solutions LLC —Guam
- $110 an hour
- Remote
- Bachelor's degree
- Quality control
- Military encouraged
Quick Apply
Proposal Writer and Copy Editor
U.S. Bank National Association —Minneapolis, MN
- $71,400 - $84,000 a year
- Full-time
- Microsoft Excel
- Marketing
- Mid-level
- Paid holidays
- Disability insurance
Contract Education Writer
The Educator's Room —Remote
- Part-time
- Remote
- School experience
- Computer literacy
- English
Quick Apply
Medical Writer, Medical Communications
Precision Medicine Group —Remote
- $80,000 - $110,000 a year
- Online Application
- Remote
- Medicine
- Doctor of Philosophy
- Negotiation
Comedy Writer
Spotter —Lemont, IL
- Remote
- English
- Mid-level
Quick Apply
2d
Technical Writer/Editor
CSSI, Inc. —Washington, DC
- Hybrid work
- High school diploma or GED
- Bachelor's degree
- Senior level
Quick Apply
Video Editor
History Factory —Remote
- Contract
- Mid-level
- Bachelor's degree
Quick Apply
Content Writer - Editor
CurvedView.com —Nashville, TN
- Email
- English
- Typing
- Entry level
Technical Content Writer
AUQ —Remote
- From $50 an hour
- Email
- Remote
- Mid-level
Technical Writer/Editor
BRS —Atlanta, GA
- Full-time
- Mid-level
- Medical terminology
- Profit sharing
- Paid holidays
Senior Technical Writer/Editor
rockITdata —Remote
- Full-time
- Computer Science
- Senior level
- Communication skills
2d

I want to receive the latest job alert for Editor/Writer

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Regulatory Writer and/or Regulatory QC/ Editor

Vir Biotechnology -
Remote

Quick Apply

Job Details

$90 - $120 an hour

Qualifications

Bachelor's degree

Full Job Description

Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN® dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.

Vir Biotechnology has exclusive rights to the universal PRO-XTEN® masking platform for oncology and infectious disease. PRO-XTEN® is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.

We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.

THE OPPORTUNITY

Vir Biotechnology is looking for a Regulatory Writer (Temporary) who will support the quality, consistency, and accuracy of regulatory documents produced by the Regulatory Writing team by either functioning as a support author and/or by focusing on editorial and QC review of documents written by other team members. Reporting to the Senior Director, Regulatory Writing, you will help ensure accuracy, compliance, and consistency of regulatory submission materials by partnering closely with medical writers, regulatory affairs, clinical, biostatistics, and other cross‑functional stakeholders.

WHAT YOU'LL DO

In partnership with an experienced lead author, write and edit a wide range of regulatory documents, including but not limited to: Clinical trial protocols and amendments, Investigator Brochures (IBs), Clinical Study Reports (CSRs), briefing packages, and components of regulatory submission dossiers (eg, NDA, IND, MAA)
Perform independent QC reviews of documents produced by the regulatory writing function
Verify the accuracy and internal/external consistency of documents versus their source materials
Define and confirm the scope of QC activities with document authors; identify required source documents/data and ensure availability prior to QC start
Review documents for adherence to applicable style guides (eg, AMA Manual of Style and internal style/formatting standards), templates, and regulatory guidance, identify and document discrepancies and recommended corrections
Proofread and copyedit text to ensure clarity, grammar, spelling, punctuation, and consistency of messaging/presentation, while preserving scientific and regulatory accuracy
Support preparation and inspection‑readiness of technical documents for global regulatory submissions (eg, eCTD/CTD), including integration of narrative text, tables, graphs, charts, and statistical output
Communicate QC findings clearly and constructively to medical writers and other stakeholders; collaborate to resolve issues and support timely completion of deliverables
Facilitate the efficient project management of individual document workflows (from KOM through handoff to publishing) and contribute to departmental trackers and integrated timelines. Communicate status and progress to stakeholders, participating in cross-functional meetings when needed
Contribute to the continuous improvement of QC tools, checklists, and processes; provide feedback on SOPs, work instructions, and best practices for regulatory document quality

WHO YOU ARE AND WHAT YOU BRING

Bachelor's degree and 5 plus years of relevant experience. Advanced degree in science or medical field is a plus
Working knowledge of the industry and content of key eCTD documents, familiarity with CTD/eCTD structure and common templates
Understanding of drug development and regulatory submission processes, including familiarity with ICH guidelines and major health authority expectations (eg, FDA, EMA)
Exceptional attention to detail with strong analytical and critical‑thinking skills, including the ability to identify inconsistencies, data issues, and deviations from standards
Proven ability to manage multiple tasks and priorities in a deadline‑driven environment, operating with a high degree of independence and accountability
Experience working cross‑functionally in collaborative team environments and building effective working relationships with authors, reviewers, and project teams
Experience with electronic document management and publishing systems (eg, Veeva Vault)
Experience with project and timeline management systems (eg, SmartSheet)

#LI-AS1

#LI-Remote

WHO WE ARE AND WHAT WE OFFER

The expected hourly range for this position is $90.00 to $120.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.

This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.

Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.

For hires based in the United States, Vir Biotechnology, participates in E-Verify.

Candidate Privacy Notice

Quick Apply

Refine Your Search

Editor/Writer jobs

Regulatory Writer and/or Regulatory QC/ Editor

Technical Writer/Editor III

Technical Writer/Editor

Technical Writer & Editor

Assistant Content Review Coordinator

Copy Editor

Content Editor / Writer with Machine Learning Experience

Writer-Editor

Writer/Editor Disney Theme Parks Content

Senior Technical Writer / Editor

Proposal Writer and Copy Editor

Contract Education Writer

Medical Writer, Medical Communications

Comedy Writer

Technical Writer/Editor

Video Editor

Content Writer - Editor

Technical Content Writer

Technical Writer/Editor

Senior Technical Writer/Editor

I want to receive the latest job alert for Editor/Writer

Related Searches

Explore jobs in more locations

THE OPPORTUNITY

WHAT YOU'LL DO

WHO YOU ARE AND WHAT YOU BRING

Job Seeker Tools

Employer Tools

Browse

Stay Connected