Top 355 Ind Us Target Jobs

Regulatory Writer and/or Regulatory QC/ Editor
Vir Biotechnology —Remote
- $90 - $120 an hour
- Remote
- 5 years
- Mid-level
- Analysis skills
Quick Apply
Principal Regulatory Writer (Temporary)
Vir Biotechnology —Remote
- $180 - $200 a day
- Temporary
- Remote
- 11+ years
- Project management
- Bachelor's degree
Quick Apply
Senior Regulatory Writer (Temporary)
Vir Biotechnology —Remote
- $130 - $170 an hour
- Temporary
- Remote
- 7 years
- Bachelor's degree
- US work authorization
Quick Apply
Sr. Director, U.S. Cancer Biology
Servier —Boston, MA
- $229,000 - $280,000 a year
- Full-time
- Writing skills
- 11+ years
- Office
- Disability insurance
- Health insurance
12d
Senior Scientist
ImmunEdge, Inc —Redwood City, CA
- $154,000 - $170,000 a year
- Full-time
- 5 years
- Doctor of Philosophy
- Senior level
- Paid holidays
- Health insurance
Quick Apply
Senior Director, US Regional Regulatory Lead
Servier —Boston, MA
- $232,000 - $284,000 a year
- Full-time
- Remote
- Management
- Bachelor of Science
- 11+ years
- Disability insurance
- Health insurance
Contract Senior Recruiter, Life Sciences
Immunome, Inc. —Bothell, WA
- $70 - $85 an hour
- Contract
- Office
- Bachelor's degree
- Organizational skills
Quick Apply
Associate Director Preclinical & Translational PK/PD
Regeneron —Tarrytown, NY
- $176,100 - $287,300 a year
- 6 years
- Math
- Doctor of Philosophy
- Health insurance
- Dental insurance
Scientist, III
BioTissue Holdings Inc —Miami, FL
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Management
- Paid parental leave
- Health savings account
Quick Apply
Regulatory Affairs Scientist
PMTS, Inc —Frederick, MD
- $85,000 - $115,000 a year
- Full-time
- Background check
- Mid-level
- Office
- Health insurance
- Dental insurance
Quick Apply
Senior Scientist - Immunotherapy
Merck KGaA —Billerica, MA
- $91,900 - $143,500 a year
- Master's degree
- Doctor of Philosophy
- Neurology
- Health insurance
- Paid time off
Vice President, Lifecycle Leader
Kyverna Therapeutics —Remote
- $300,000 - $340,000 a year
- Full-time
- Remote
- Medicine
- 11+ years
- Doctor of Philosophy
Precision Medicine Global Biomarker Lead , Rare Disease
Amgen —Remote
- $166,523.50 - $225,296.50 a year
- Remote
- Medicine
- 3 years
- Bachelor's degree
- Disability insurance
- Health insurance
14d
Manager, Regulatory Affairs
Jade Biosciences —Seattle, WA
- $135,000 - $150,000 a year
- Remote
- Microsoft Word
- 3 years
- Bachelor's degree
Quick Apply
Director, Toxicology
Pliant Therapeutics, Inc. —South San Francisco, CA
- $232,000 - $256,000 a year
- Full-time
- Doctor of Philosophy
- Senior level
- Communication skills
Quick Apply
Associate Director, Toxicology
Protagonist Therapeutics —Newark, CA
- $185,000 - $205,000 a year
- Project management
- Doctor of Philosophy
- Pediatrics
Quick Apply
Senior Licensed Architect
Huitt-Zollars —Philadelphia, PA
- Full-time
- Office
- US work authorization
- Computer skills
- Commuter assistance
- AD&D insurance
Quick Apply
Senior Licensed Architect - Institutional
Huitt-Zollars —Houston, TX
- Full-time
- Office
- Travel
- US work authorization
- Commuter assistance
- AD&D insurance
Quick Apply
Civil Engineer Design-Build Leader – Vice President / Principal-in-Charge
Huitt-Zollars —Dallas, TX
- Full-time
- Office
- Bachelor's degree
- Travel
- Commuter assistance
- AD&D insurance
Quick Apply
Senior Project Manager – Licensed Site Professional (LSP)
Pinchin LLC —North Andover, MA
- 7 years
- Management
- Master's degree
- Health savings account
- Flexible spending account
Quick Apply

I want to receive the latest job alert for Ind Us Target

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

Ind Us Target jobs

Regulatory Writer and/or Regulatory QC/ Editor

Principal Regulatory Writer (Temporary)

Senior Regulatory Writer (Temporary)

Sr. Director, U.S. Cancer Biology

Senior Scientist

Senior Director, US Regional Regulatory Lead

Contract Senior Recruiter, Life Sciences

Associate Director Preclinical & Translational PK/PD

Scientist, III

Regulatory Affairs Scientist

Senior Scientist - Immunotherapy

Vice President, Lifecycle Leader

Precision Medicine Global Biomarker Lead , Rare Disease

Manager, Regulatory Affairs

Director, Toxicology

Associate Director, Toxicology

Senior Licensed Architect

Senior Licensed Architect - Institutional

Civil Engineer Design-Build Leader – Vice President / Principal-in-Charge

Senior Project Manager – Licensed Site Professional (LSP)

I want to receive the latest job alert for Ind Us Target

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