ZipRecruiter

Log In

1

Senior Science Communication Jobs in California (NOW HIRING)

ManTech

Senior Science and Research Analyst

Livermore, CA

$104K - $172K/yr

  • Medical

  • Life

  • Retirement

  • PTO

The Senior Science and Research Analyst will leverage their strong technical background and ... Self-starter with excellent communication and interpersonal skills, capable of building consensus ...

New

Eurofins

Senior Scientist, Analytical Development

Fremont, CA · On-site

$100K - $136K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Senior Scientist, Analytical Development Duties Include but are not Limited to the Following ... Data Analysis and Scientific Communication * Analyze, interpret, and present assay data using ...

Biogen

Senior Scientist, Immunology

San Francisco, CA

$107K - $147K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Communicate scientific findings effectively through internal presentations, cross-functional ... senior scientific leaders, business development, and corporate strategy teams, as appropriate.

Biogen

Senior Scientist, Immunology

San Francisco, CA · On-site

$107K - $147K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Communicate scientific findings effectively through internal presentations, cross-functional ... senior scientific leaders, business development, and corporate strategy teams, as appropriate.

next page

Showing results 1-20

All JobsScience Communication JobsSenior Science Communication JobsSenior Science Communication Jobs in California

Senior Science Communication information

What is the difference between Senior Science Communication vs Science Writer?

AspectSenior Science CommunicationScience Writer
Required CredentialsAdvanced degree in science or communication, experience in science outreachDegree in journalism, communications, or related field; strong writing skills
Work EnvironmentResearch institutions, science centers, universities, public outreachMedia outlets, publishing companies, online platforms
Employer & Industry UsageUsed in academia, government agencies, science museumsCommon in media, publishing, science journalism

While both roles involve communicating science, Senior Science Communication focuses on strategic outreach and public engagement, often within institutions. Science Writers primarily produce articles, reports, and content for media outlets. The roles overlap in communication skills but differ in scope and environment.

What are the most commonly searched types of Science Communication jobs in California?

The most popular types of Science Communication jobs in California are:

What are popular job titles related to Senior Science Communication jobs in California?

For Senior Science Communication jobs in California, the most frequently searched job titles are:

What job categories do people searching Senior Science Communication jobs in California look for?

The top searched job categories for Senior Science Communication jobs in California are:

What cities in California are hiring for Senior Science Communication jobs?

Cities in California with the most Senior Science Communication job openings:

Senior Science Communication jobs near you

Senior Director, Regulatory Science Communication

Kardigan

South San Francisco, CA

$180K - $237K/yr

Full-time

Re-posted 3 days ago

Job description

Position Title: Senior Director, Regulatory Science Communication

Department: Regulatory

Reports To: SVP, Head of Regulatory

Location: South San Francisco, CA or Princeton, NJ 

Job Overview

The Senior Director, Regulatory Science Communication is a strategic leadership role responsible for the development, alignment, and execution of high-impact regulatory communication strategies. This individual leads the development of clear, scientifically rigorous, and compliant regulatory content that supports health authority interactions, product approvals, and lifecycle management globally. This role serves as a key partner to Regulatory Affairs, Clinical Development, Biostatistics, Pharmacovigilance, and other cross-functional stakeholders. The Senior Director is expected to provide both strategic direction and hands-on leadership across document planning, content development, review and approval.

Essential Duties and Responsibilities

Key Responsibilities

  • Lead the strategic development and execution of integrated regulatory science communication plans across the product lifecycle
  • Align communication strategies with overall regulatory objectives, clinical development plans, and benefit-risk assessments
  • Provide strategic oversight and, as needed, direct authoring support for critical regulatory documents, ensuring they are fit for purpose, scientifically sound, and compliant with global regulatory standards
  • Oversee development of key regulatory content, including briefing documents, response packages, eCTD Module 2 summaries and overviews, protocols and protocol amendments, clinical study reports (CSRs), and responses to health authority questions
  • Partner with regulatory leaders and cross-functional teams to ensure that submission documents reflect a clear, persuasive, and evidence-based scientific narrative that accurately interprets complex clinical, statistical, and safety data for regulatory audiences
  • Establish and continuously improve standards, templates, style guides, and content frameworks that support efficient, high-quality regulatory document development.
  • Champion the thoughtful use of digital and AI-enabled tools to improve document planning, content development, and review workflows while maintaining scientific integrity and compliance
  • Ensure that regulatory communications meet GxP, inspection-readiness, and documentation standards appropriate for global development and submission activities
  • Provide leadership, coaching, and direction to internal writers, external vendors, and contract medical or regulatory writers as applicable.

Qualifications and Preferred Skills

  • Advanced degree preferred (PhD, PharmD, MD, or equivalent in life sciences or related discipline)
  • 10+ years of experience in regulatory affairs, regulatory writing, medical writing, or scientific communication
  • Demonstrated experience supporting global regulatory submissions and health authority interactions across development stages
  • Strong expertise in development of regulatory documentation, including briefing books, eCTD content, clinical summaries, protocols, CSRs, and health authority responses
  • Deep understanding of global regulatory frameworks and guidelines, including FDA, EMA, and ICH requirements
  • Proven ability to influence senior cross-functional stakeholders to drive alignment

Apply