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Director Real World Evidence Rwe Jobs in California

Syneos Health, Inc.

Clinical Value Liaison

San Francisco, CA · On-site

$235K - $246K/yr

... real-world evidence (RWE), health economics and outcomes research (HEOR), and value-based care. The ... Establish and maintain scientific relationships with payer medical directors, pharmacy directors ...

Syneos Health Careers

Clinical Value Liaison

Los Angeles, CA · On-site

$235K - $246K/yr

... real-world evidence (RWE), health economics and outcomes research (HEOR), and value-based care. The ... Establish and maintain scientific relationships with payer medical directors, pharmacy directors ...

Syneos Health

Clinical Value Liaison

Los Angeles, CA · On-site

$235K - $246K/yr

... real-world evidence (RWE), health economics and outcomes research (HEOR), and value-based care. The ... Establish and maintain scientific relationships with payer medical directors, pharmacy directors ...

Syneos Health, Inc.

Clinical Value Liaison

Los Angeles, CA · On-site

$235K - $246K/yr

... real-world evidence (RWE), health economics and outcomes research (HEOR), and value-based care. The ... Establish and maintain scientific relationships with payer medical directors, pharmacy directors ...

Travere

Senior Biostatistician

San Diego, CA · On-site +1

... Director, Biostatistics in providing statistical support to Health Economics and Outcomes Research (HEOR), Real World Evidence (RWE), and Market Access activities in support of drug development and ...

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Director Real World Evidence Rwe information

What is the difference between Director Real World Evidence Rwe vs Clinical Data Manager?

AspectDirector Real World Evidence RweClinical Data Manager
CredentialsAdvanced degrees (PhD, MD, or Master’s), industry certificationsBachelor’s or Master’s in life sciences, clinical research
Work EnvironmentStrategic, cross-functional teams, senior managementData collection, database management, clinical trial sites
Industry UsagePharmaceuticals, biotech, healthcare analyticsClinical research organizations, pharmaceutical companies

The main difference is that the Director Real World Evidence Rwe focuses on designing and leading real-world data studies to inform healthcare decisions, while the Clinical Data Manager handles the collection and management of clinical trial data. The Rwe director has a broader strategic role, whereas the Clinical Data Manager is more operational and detail-oriented.

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Director Real World Evidence Rwe jobs near you
Infographic showing various Director Real World Evidence Rwe job openings in California as of September 2026, with employment types broken down into 1% Internship, 75% Full Time, 21% Part Time, 1% Temporary, and 2% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution.

Director, Medical Communications

Palo Alto, CA • On-site

Summit Therapeutics
See more jobs at Summit Therapeuticsexternal

Full-time

Posted 19 days ago

Job description

Overview of Role:

Director, Medical Communications will lead the development and execution of a comprehensive medical communications strategy, ensuring alignment across internal and external stakeholders for ivonescimab with focus on NSCLC, CRC, and other solid tumors. This role will oversee and manage scientific communications platforms and contribute to medical content supporting the organization's medical and scientific engagement efforts.

This is an onsite role based in Palo Alto, CA. This position will report to the Senior Director, Medical Communications and Information.

Role and Responsibilities:

  • Design, implement, and maintain global medical communications strategy supporting product launches, lifecycle management, and scientific engagement ensuring consistency, clarity, and scientific rigor across all external and internal communications.
  • Create the scientific communications platform and core scientific narratives to guide consistent, high impact messaging.
  • Oversee development of scientifically accurate medical content across education programs, training materials, digital channels, symposia, RMSD tools, and congresses.
  • Ensure consistency and alignment of medical messaging across all communication channels and materials.
  • Collaborate cross-functionally with Medical Affairs (e.g., Field Medical (RMSDs), Patient Advocacy, Training, Medical Information and Medical Education), Regulatory, Clinical Development, and Commercial partners across the organization to ensure alignment and accuracy in messaging and to ensure a cohesive medical communications and engagement strategy.
  • Partner with external agencies, key opinion leaders, and scientific experts to strengthen relevance and impact.
  • Lead, mentor, and develop medical writers and communication specialists, driving quality, compliance, and timely delivery.
  • Manage and support centralized reference library for scientific decks, field medical materials (RMSD tools), medical booth content, infographics, videos, and other external engagement materials.
  • Drive scientific congress planning and execution, including coordination of symposia, abstracts/posters and presentations.
  • Identify opportunities to amplify scientific presence at major oncology congresses.
  • All other duties as assigned 

 

Experience, Education and Specialized Knowledge and Skills:

  • Advanced scientific or medical degree (PhD, PharmD, MD) with 8+ years of experience in Medical Affairs, Medical Communications within the biotechnology or pharmaceutical industry; MS or equivalent experience in biomedical sciences or related field considered.
  • Experience in oncology, specifically NSCLC and CRC.
  • Deep understanding of industry guidelines, and best practices (PhRMA Code, GPP 2022, FDA, OIG, AdvaMed, Sunshine Act).
  • Proven ability to develop and execute medical communication strategies aligned with company and scientific priorities.
  • Familiarity with clinical development and real-world evidence (RWE) and how these influence scientific communication strategies.
  • Ability to manage external agency relationships, medical writers, and vendors to ensure quality and compliance in content development.
  • Ability to translate complex scientific data into clear, engaging, and compliant communications for different stakeholders.
  • Ability to work in fast-paced, matrixed environments and lead cross-functional initiatives.
  • Strong project management skills to oversee multiple priorities, timelines, and stakeholders effectively.
  • Excellent communication, interpersonal, and presentation skills to engage internal and external stakeholders effectively.

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