Top 2016 Writer / Director Jobs

Regulatory Writer and/or Regulatory QC/ Editor
Vir Biotechnology —Remote
- $90 - $120 an hour
- Remote
- 5 years
- Mid-level
- Analysis skills
Quick Apply
Grants Writer
Thrive —Bozeman, MT
- From $30 an hour
- Part-time
- Mid-level
- Children
- Organizational skills
- Paid time off
Quick Apply
1d
Director of Development
Lussier Community Education Center —Madison, WI
- Up to $74,000 a year
- Weekends as needed
- CRM software
- Background check
- Spanish
- Health savings account
- Disability insurance
Quick Apply
2d
Director of Strategic Partnerships
Center for Creative Education —West Palm Beach, FL
- $80,000 - $90,000 a year
- Weekends as needed
- Background check
- Research
- Office
- Paid holidays
- Disability insurance
Quick Apply
Director of Institutional Giving
Healing New York —New York, NY
- $125,000 a year
- Email
- Hybrid work
- 6 years
- Office
- Bachelor's degree
- 403(b) matching
- Health savings account
Quick Apply
Executive Director
North East Community Center —Millerton, NY
- $110,000 - $125,000 a year
- Email
- Background check
- Spanish
- Ability to climb stairs
- Health insurance
- 401(k)
Quick Apply
7d
Director of Institutional Giving
Boston Arts Academy Foundation —Boston, MA
- $90,000 - $110,000 a year
- Email
- Hybrid work
- 7 years
- Microsoft Excel
- High school
- Paid holidays
- Health insurance
Quick Apply
Development Associate
Community Health Initiative, Napa County —Napa, CA
- $72,000 - $80,000 a year
- Weekends as needed
- Google Workspace
- Research
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred
Syneos - Clinical and Corporate - Prod —New Jersey
- $95,000 - $210,900 a year
- Full-time
- Microsoft Word
- 5 years
- Bachelor's degree
- Employee stock purchase plan
- Health insurance
Chief Development Officer (CDO)
Door of Hope —Pasadena, CA
- $165,000 - $190,000 a year
- Weekends as needed
- Office
- In-person
- Senior level
- Paid jury duty
- Health insurance
Quick Apply
Transportation Manager
KETCHIKAN INDIAN CORPORATION —Ketchikan, AK
- Full-time
- Clean driving record
- Customer service
- Computer literacy
Senior Director of Information Security & Deputy CISO
MLMIC SERVICES, INC —New York State
- $202,300 - $274,900 a year
- Full-time
- Computer Science
- Word processing
- 11+ years
- Paid holidays
- Disability insurance
Quick Apply
Master's Level Clinician/Therapist
Justice Resource Institute —Taunton, MA
- $63,000 - $68,000 a year
- Licensed Clinical Social Worker
- Residential
- Driver's License
Quick Apply
SPED Teacher (Special Needs)
Creative Minds CDC —Paducah, KY
- $14 - $17 an hour
- Full-time
- Background check
- Classroom
- CPR Certification
- 401(k)
- Paid time off
Quick Apply
Director of Nursing
Elwyn —Walnut Creek, CA
- $115,000 - $140,000 a year
- Nursing
- Clean driving record
- Microsoft Excel
- Paid training
- Health insurance
Quick Apply
Director of Grant Development
World Concern —Shoreline, WA
- $100,000 - $150,000 a year
- Full-time
- 7 years
- Research
- Office
- Paid holidays
- Health insurance
Quick Apply
Artist in Residence
Ruakh Arts —Ashland, VA
- $1,000 a month
- Weekends as needed
- Background check
- Residential
- Bachelor's degree
- Paid training
- Professional development assistance
Quick Apply
School Social Worker
Lighthouse Academy/Integrity Educational Services —Grand Rapids, MI
- $60,000 - $68,000 a year
- Full-time
- Background check
- Classroom
- Master of Social Work
- Health savings account
- Health insurance
Quick Apply
7d
Multi-Media Journalist/News Reporter
WPSD-TV —Paducah, KY
- Full-time
- Driver's License
- In-person
- Editing
- Health insurance
- Dental insurance
Quick Apply
Director of Development
Community Counseling and Mediation —Brooklyn, NY
- $83,000 - $93,000 a year
- Full-time
- Addiction Medicine
- 5 years
- Research
- Commuter assistance
- Health insurance
Quick Apply

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

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

Writer / Director jobs

Regulatory Writer and/or Regulatory QC/ Editor

Grants Writer

Director of Development

Director of Strategic Partnerships

Director of Institutional Giving

Executive Director

Director of Institutional Giving

Development Associate

Sr. Principal Medical Writer - Regulatory Submission Docs (ISE/ISS/Clinical Overview - Must Have) - Oncology Preferred

Chief Development Officer (CDO)

Transportation Manager

Senior Director of Information Security & Deputy CISO

Master's Level Clinician/Therapist

SPED Teacher (Special Needs)

Director of Nursing

Director of Grant Development

Artist in Residence

School Social Worker

Multi-Media Journalist/News Reporter

Director of Development

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

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