Top 1328 Sr development editor Jobs

Regulatory Writer and/or Regulatory QC/ Editor
Vir Biotechnology —Remote
- $90 - $120 an hour
- Remote
- 5 years
- Mid-level
- Analysis skills
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Senior Ontologist
Johns Hopkins Applied Physics Laboratory (APL) —Laurel, MD
- $100,000 - $245,000 a year
- Full-time
- Computer Science
- Master's degree
- Analysis skills
- Disability insurance
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Senior Ontologist (TS/SCI cleared)
Johns Hopkins Applied Physics Laboratory (APL) —Laurel, MD
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Senior Manager of Public Relations
Boston Athletic Association —Boston, MA
- $82,500 - $87,500 a year
- Weekends as needed
- Hybrid work
- 5 years
- Travel
- Organizational skills
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- Paid holidays
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1d
Senior Non-Clinical Editor
Kaztronix —Wilmington, DE
- Contract
- Remote
- Microsoft Word
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5d
Technical Editor, MID
Amentum —Reston, VA
- $100,000 - $115,000 a year
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- 3 years
- Health insurance
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Sr. Technical Editor
General Dynamics Information Technology —Bethesda, MD
- $81,349 - $109,250 a year
- Microsoft Excel
- 5 years
- Bachelor's degree
- Paid time off
- 401(k) matching
Technical Editor/Data Manager
CACI —Albuquerque, NM
- $58,500 - $122,800 a year
- Full-time
- Microsoft Access
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- Bachelor of Science
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Senior Quotations Specialist
REXEL —Orlando, FL
- Full-time
- Microsoft Outlook
- 5 years
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8d
Senior Designer
ESPN —Bristol, CT
- $87,100 - $116,800 a year
- 6 years
- High school diploma or GED
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Deputy Press Secretary – Bilingual
New York City Council —New York, NY
- $80,000 - $95,000 a year
- Weekends as needed
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- Spanish
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Sr Principal Engineer Electronics
Northrop Grumman —Chandler, AZ
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- 3 years
- Master's degree
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14d
Multiple Positions for Communications Security Directorate (CSD)
General Dynamics Information Technology —Fort Huachuca, AZ
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- Multiple hires
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- 3 years
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- 401(k) matching
Lead Designer – Client Services, Strategic Capital
Prologis —New York, NY
- $91,000 - $125,000 a year
- Full-time
- Hybrid work
- 7 years
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Principal Digital Hardware Design Engineer -Onsite
Raytheon —McKinney, TX
- $107,500 - $204,500 a year
- Full-time
- Laboratory experience
- 8 years
- Analysis skills
- Paid holidays
- Disability insurance
14d
Senior Digital Hardware Design Engineer - Onsite
Raytheon —McKinney, TX
- $86,800 - $165,200 a year
- Full-time
- 5 years
- Laboratory experience
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- Paid holidays
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14d
Director, Brand PR (Onsite - Boca Raton, FL)
Braintrust —Los Angeles, CA
- $180,000 - $200,000 a year
- 11+ years
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14d
Senior Architectural Project Manager
Supreme Staffing —Brooklyn, NY
- $120,000 - $160,000 a year
- Full-time
- AutoCAD
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- 5 years
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19h
Copy Editor
Cognition Learning Group —Remote
- $142 - $213 a day
- Contract
- Remote
- English
- Mid-level
12d
Technical Writer/Editor
Artemis Arc —Remote
- Remote
- Microsoft Excel
- English
- Mid-level
5d

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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

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Refine Your Search

sr development editor jobs

Regulatory Writer and/or Regulatory QC/ Editor

Senior Ontologist

Senior Ontologist (TS/SCI cleared)

Senior Manager of Public Relations

Senior Non-Clinical Editor

Technical Editor, MID

Sr. Technical Editor

Technical Editor/Data Manager

Senior Quotations Specialist

Senior Designer

Deputy Press Secretary – Bilingual

Sr Principal Engineer Electronics

Multiple Positions for Communications Security Directorate (CSD)

Lead Designer – Client Services, Strategic Capital

Principal Digital Hardware Design Engineer -Onsite

Senior Digital Hardware Design Engineer - Onsite

Director, Brand PR (Onsite - Boca Raton, FL)

Senior Architectural Project Manager

Copy Editor

Technical Writer/Editor

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