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Science Communication Jobs in California (NOW HIRING)

Quantitative Biologist

Emeryville, CA · On-site +1

$150K - $200K/yr

They have strong intuitions about image data, high expectations for rigorous experimental design, and the communication skills to make quantitative reasoning accessible to scientists with diverse ...

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Science Communication information

See California salary details

$19.2K

$48.4K

$70.1K

How much do science communication jobs pay per year?

As of Jul 6, 2026, the average yearly pay for science communication in California is $48,421.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,000.00 and $54,800.00 per year, depending on experience, location, and employer.

What types of projects or content do Science Communication professionals typically work on?

Science Communication professionals often create a wide variety of content including articles, press releases, social media posts, multimedia presentations, infographics, and educational resources. They may also organize public lectures, outreach events, or collaborate on video and podcast production. Typically, they work closely with scientists, educators, and media teams to ensure accurate and engaging messaging. The role requires balancing scientific accuracy with accessibility for non-expert audiences, making it both challenging and intellectually rewarding.

What are the key skills and qualifications needed to thrive in the Science Communication position, and why are they important?

To excel in Science Communication, you need a solid foundation in scientific knowledge, excellent written and verbal communication abilities, and typically a relevant degree in science or communications. Familiarity with digital publishing platforms, social media management tools, and sometimes science writing certifications are commonly required. Strong interpersonal skills, creativity, and the ability to distill complex concepts into engaging content set standout candidates apart. These skills ensure scientific information is accurately and compellingly communicated to diverse audiences, facilitating better public understanding and engagement.

What is a Science Communication job?

A Science Communication job involves translating complex scientific concepts into clear, engaging, and accessible information for the public, policymakers, or specific audiences. Professionals in this field work in media, education, research institutions, or governmental organizations, using various formats like articles, social media, videos, and public talks. The goal is to bridge the gap between scientists and the public, ensuring accurate and compelling science storytelling.

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 cities in California are hiring for Science Communication jobs? Cities in California with the most Science Communication job openings:

Senior Director, Regulatory Science Communication

Kardigan

South San Francisco, CA

$180K - $237K/yr

Other

Posted 24 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 - On site 4 days a week (Mon to Thurs)

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