Top 388 Disease investigator Jobs in California

Regulatory Writer and/or Regulatory QC/ Editor
Vir Biotechnology —San Francisco, CA
- $90 - $120 an hour
- Remote
- 5 years
- Mid-level
- Analysis skills
Quick Apply
Public Health Field Investigator
Council For Logistics Research Inc —San Diego, CA
- $85,000 - $105,000 a year
- Full-time
- Nursing
- Mid-level
- Bachelor's degree
- Health insurance
- Dental insurance
10d
Research Pharmacist (Per Diem - Investigational Drug Service)
Folio Clinical Research —Bakersfield, CA
- $75 - $110 an hour
- Part-time
- Mid-level
- Clinic
- Patient care
Quick Apply
Clinical Research Advanced Nurse Practitioner/Physcian Assistant
Houston Research Institute —Los Angeles, CA
- $140,000 - $160,000 a year
- Full-time
- Experience working with individuals with developmental disabilities
- Nursing
- Medication administration
- Health insurance
- Dental insurance
Quick Apply
Associate Director, Global Clinical Scientist (Cell Therapy)
BMS —Brisbane, CA
- $184,270 - $256,789 a year
- Email
- Hybrid work
- Medicine
- Microsoft Excel
- 5 years
- Paid holidays
- Disability insurance
Senior Manager, Global Clinical Scientist (Cell Therapy)
BMS —Brisbane, CA
- $150,770 - $210,110 a year
- Email
- Hybrid work
- Microsoft Word
- Medicine
- Microsoft Excel
- Paid holidays
- Disability insurance
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
Senior Medical Science Liaison, Inborn Errors of Metabolism (Atlantic Region)
Ultragenyx Pharmaceutical —Novato, CA
- $195,600 - $241,600 a year
- Full-time
- Remote
- Medicine
- Presentation skills
- Doctor of Philosophy
- Gym membership
Clinical Research Coordinator Infectious Disease
University of California San Francisco —San Francisco, CA
- Full-time
- Spanish
- Microsoft Outlook
- Bachelor of Science
Disease-focused Neuroscience and Translational Neurobiology Faculty Position | Gladstone Institutes and UCSF
Gladstone Institutes —San Francisco, CA
- $250,000 - $350,000 a year
- Online Application
- Medicine
- Doctoral degree
- Residential
- Commuter assistance
- Health insurance
Assistant Researcher
UCLA —Los Angeles, CA
- $96,700 - $114,300 a year
- Online Application
- Psychiatry
- Analysis skills
- University
Disease Team Project Manager - Cancer Center
UC San Diego Health —San Diego, CA
- $46.55 - $87.16 an hour
- 8 hour shift
- Hybrid work
- 5 years
- Word processing
- Pass drug screening
6d
Program Coordinator I
San Diego State University Research Foundation —San Diego, CA
- $5,875 a month
- Full-time
- Remote
- Background check
- Spanish
- 5 years
Assistant Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Windows
- High school diploma or GED
- 21 years or older
10d
Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Full-time
- HIPAA
- High school diploma or GED
- University
Administrative Officer 2
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Excel
- Mid-level
- Windows
Clinical Research Coordinator
University of California, Irvine —Irvine, CA
- $35.77 - $58.96 an hour
- Full-time
- Background check
- Microsoft Access
- Hospital
- Health insurance
- Retirement plan
Animal Resources Supervisor
University of California San Francisco —San Francisco, CA
- Weekends as needed
- Computer literacy
- Mid-level
- University
2d
Sub Investigator
Velocity Clinical Research, Inc. —Los Angeles, CA
- Full-time
- Medicine
- 5 years
- HIPAA
- Paid holidays
- Health insurance
Quick Apply
Clinical Reseach Coordinator
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Excel
- HIPAA
- Mid-level
4d

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Regulatory Writer and/or Regulatory QC/ Editor

Vir Biotechnology -
San Francisco, CA

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

disease investigator jobs in california

Regulatory Writer and/or Regulatory QC/ Editor

Public Health Field Investigator

Research Pharmacist (Per Diem - Investigational Drug Service)

Clinical Research Advanced Nurse Practitioner/Physcian Assistant

Associate Director, Global Clinical Scientist (Cell Therapy)

Senior Manager, Global Clinical Scientist (Cell Therapy)

Director of Nursing

Senior Medical Science Liaison, Inborn Errors of Metabolism (Atlantic Region)

Clinical Research Coordinator Infectious Disease

Disease-focused Neuroscience and Translational Neurobiology Faculty Position | Gladstone Institutes and UCSF

Assistant Researcher

Disease Team Project Manager - Cancer Center

Program Coordinator I

Assistant Clinical Research Coordinator

Clinical Research Coordinator

Administrative Officer 2

Clinical Research Coordinator

Animal Resources Supervisor

Sub Investigator

Clinical Reseach Coordinator

I want to receive the latest job alert for disease investigator in california

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