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Real World Evidence Rwe Jobs in California (NOW HIRING)

AOTI

Payroll Specialist

Oceanside, CA · On-site +1

$34 - $37/hr

... Real-World Evidence (RWE) studies. TWO2 has delivered exceptional clinical outcomes, including an 88% reduction in hospitalizations and a 71% reduction in amputations among patients with Diabetic ...

AOTI

Payroll Specialist

Oceanside, CA · On-site

$34 - $37/hr

... Real-World Evidence (RWE) studies. TWO2 has delivered exceptional clinical outcomes, including an 88% reduction in hospitalizations and a 71% reduction in amputations among patients with Diabetic ...

Penumbra

Market Access Analytics Manager

Alameda, CA · On-site

... for Real-World Evidence data analysis reports and tools throughout the process of collection, analysis, and submission of RWE data. • Develops skills and shares them with others. • Provide ...

Penumbra

Market Access Analytics Manager

Alameda, CA · On-site +1

Follow data standards policies, procedures, practices, and regulations for Real-World Evidence data analysis reports and tools throughout the process of collection, analysis, and submission of RWE ...

IQVIA

Senior Global Client Partner

San Francisco, CA · Remote

... Real World Evidence, and related services. They collaborate closely with the rest of the Global ... Align the account asset strategy with RDS & RWE to ensure a joined up 'Molecule to Market ...

IQVIA

Senior Global Client Partner

San Francisco, CA · Remote

... Real World Evidence, and related services. They collaborate closely with the rest of the Global ... Align the account asset strategy with RDS & RWE to ensure a joined up 'Molecule to Market ...

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Real World Evidence Rwe information

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

AspectReal World Evidence RweClinical Data Analyst
Required credentialsTypically requires a background in healthcare, epidemiology, or biostatistics, often with a master's or PhDUsually requires a degree in health informatics, biostatistics, or related fields, with similar certifications
Work environmentPrimarily in healthcare, pharmaceutical, or research organizations analyzing real-world dataIn clinical research settings, hospitals, or pharmaceutical companies analyzing clinical trial data
Employer and industry usageUsed by pharma companies, healthcare providers, and research institutions to generate real-world insightsUsed by research organizations, hospitals, and pharma for clinical trial data management and analysis

Real World Evidence Rwe professionals focus on analyzing data from real-world settings like electronic health records and insurance claims, while Clinical Data Analysts primarily work with clinical trial data. Both roles require strong analytical skills and related credentials, but Rwe specialists emphasize real-world data sources to inform healthcare decisions.

What jobs are there in clinical trials?

Jobs in clinical trials include Clinical Research Coordinators, Clinical Data Managers, Clinical Research Associates, and Study Monitors. These roles involve tasks such as patient recruitment, data collection, monitoring trial progress, and ensuring compliance with regulations, often requiring knowledge of Good Clinical Practice (GCP) and relevant certifications. The work environment is typically in hospitals, research centers, or pharmaceutical companies, with schedules varying from standard to flexible hours.

What is RCT and RWE?

In the context of a Real World Evidence (RWE) role, RCTs (Randomized Controlled Trials) are clinical studies that randomly assign participants to different treatments to assess efficacy, while RWE involves analyzing data from real-world settings like electronic health records and insurance claims to evaluate treatment effectiveness outside controlled trials. Both are important for informing healthcare decisions and regulatory approvals, with RWE complementing RCT data by providing insights from everyday clinical practice.

What is Real World Evidence (RWE) in the healthcare industry?

Real World Evidence (RWE) refers to clinical evidence regarding the usage and potential benefits or risks of a medical product, derived from analysis of real-world data (RWD). This data is collected from sources outside of traditional clinical trials, such as electronic health records, insurance claims, patient registries, and wearable devices. RWE plays a crucial role in understanding how treatments work in routine clinical practice, informing regulatory decisions, and supporting drug development and market access. Organizations use RWE to complement clinical trial data, improving healthcare outcomes and patient care.

What are the roles in clinical trials?

In clinical trials, roles include Principal Investigator who oversees the study, Study Coordinators who manage daily operations, Data Managers who handle data collection and analysis, and Regulatory Affairs Specialists who ensure compliance with regulations. These roles require specific skills, certifications, and knowledge of Good Clinical Practice (GCP) guidelines to ensure the trial's integrity and participant safety.

What are the key skills and qualifications needed to thrive as a Real World Evidence (RWE) professional, and why are they important?

To thrive as a Real World Evidence (RWE) professional, you need a strong background in epidemiology, biostatistics, and data analysis, often supported by an advanced degree in a relevant scientific field. Familiarity with statistical software (such as SAS, R, or Python), real-world data sources (like EHRs and claims databases), and regulatory guidelines (FDA/EMA) is essential. Strong communication, problem-solving, and cross-functional collaboration skills help convey complex findings to stakeholders and integrate RWE into decision-making. These competencies are crucial for generating credible insights that inform clinical, regulatory, and commercial strategies in the healthcare industry.

How does a Real World Evidence (RWE) professional typically collaborate with cross-functional teams in the pharmaceutical industry?

RWE professionals often work closely with colleagues from epidemiology, health economics, medical affairs, and regulatory affairs to design and execute studies using real-world data. Collaboration is essential, as RWE findings support evidence generation for regulatory submissions, market access, and post-marketing surveillance. Regular meetings, data-sharing sessions, and joint project planning are common, ensuring all stakeholders are aligned on study objectives, methodologies, and data interpretation. This collaborative environment helps translate complex data into actionable insights that support decision-making across the organization.

What is RWE in clinical research?

Real World Evidence (RWE) in clinical research refers to data collected from real-world settings outside controlled clinical trials, such as electronic health records, insurance claims, and patient registries. RWE helps researchers and healthcare professionals understand how treatments perform in routine practice and supports decision-making for drug development and regulatory approval.
What are the most commonly searched types of Real World Evidence Rwe jobs in California? The most popular types of Real World Evidence Rwe jobs in California are:
What are popular job titles related to Real World Evidence Rwe jobs in California? For Real World Evidence Rwe jobs in California, the most frequently searched job titles are:
What job categories do people searching Real World Evidence Rwe jobs in California look for? The top searched job categories for Real World Evidence Rwe jobs in California are:
What cities in California are hiring for Real World Evidence Rwe jobs? Cities in California with the most Real World Evidence Rwe job openings:
Real World Evidence Rwe jobs near you
Infographic showing various Real World Evidence Rwe job openings in California as of July 2026, with employment types broken down into 70% Full Time, and 30% Part Time. Highlights an 72% In-person, 14% Hybrid, and 14% Remote job distribution.
Executive Director, Global Scientific Communications

Executive Director, Global Scientific Communications

Revolution Medicines

Redwood City, CA • On-site, Remote

Other

Re-posted 2 days ago

Job description

The Opportunity:

As a new member of the Revolution Medicines team, the Executive Director, Global Scientific Communications will lead the development and execution of a comprehensive scientific communications strategy and team, ensuring alignment across internal and external stakeholders in preparation for the company's first commercial launch in pancreatic cancer and the progression of additional pipeline assets in NSCLC, colorectal cancer, and other solid tumors.

Reporting into the SVP, Global Medical Affairs, this role will will be responsible for leading our scientific communications platforms and publication strategies and contribute to medical content supporting the organization's medical and scientific engagement efforts.

Key responsibilities include:

Publications Strategy & Execution

  • Lead the development and execution of the global publication plans, ensuring alignment with clinical and scientific objectives.

  • Oversee and provide strategic direction for medical writing, publication planning meetings, the submission process, and timely/high-quality scientific communications and publications.

  • Ensure compliance with Good Publication Practices (GPP), ICMJE guidelines, and industry standards.

  • Manage and optimize the use of Datavision or other publication management systems to ensure visibility, collaboration, and compliance across teams.

Scientific Communications Platform

  • Develop and maintain the scientific narrative and core communication messages for pipeline programs.

  • Oversee creation of scientific platform materials to ensure consistency and scientific integrity in external communications.

  • Ensure alignment with Medical, Clinical, and Commercial teams for accurate and impactful messaging.

Congress Strategy & Scientific Exchange

  • Drive scientific congress planning and execution, including coordination of symposia, abstracts/posters, presentations, and medical booth presence.

  • Identify opportunities to amplify Revolution Medicines' scientific presence at major oncology congresses (e.g., ASCO, ESMO, AACR).

Internal Education & Change Management

  • Implement change management strategies to enhance internal understanding of best practices in publications strategy and execution.

  • Educate internal stakeholders on scientific publication standards, compliance requirements, and best-in-class medical communication practices.

  • Build trust across the organization in the Medical Communications function, reinforcing its role as the central authority on publication strategy, planning, and execution.

Cross-functional Collaboration & Leadership

  • Serve as a key member of the Medical Excellence team, contributing to medical strategy and launch planning.

  • Partner with Field Medical (MSLs), Medical Information, and Medical Education to ensure a cohesive medical communications and engagement strategy.

  • Work with internal and external stakeholders to contribute to educational content for KOLs, HCPs, and internal teams.

Required Skills, Experience and Education:

  • Advanced scientific or medical degree (PhD, PharmD, MD) required

  • 15+ years of experience in Medical Affairs, Medical Communications and publications planning/execution within the biotechnology or pharmaceutical industry.

  • Experience leading scientific publication strategy, medical education initiatives, and external stakeholder engagement.

  • Experience leading a Medical Affairs-focused team

  • Deep understanding of industry guidelines, and best practices (ACCME, PhRMA Code, FDA, OIG, AdvaMed, Sunshine Act).

  • Proven ability to develop and execute medical communication strategies aligned with company and scientific priorities.

  • Expertise in scientific communications planning, data dissemination, and medical writing/publication processes, including authorship guidelines (ICMJE, GPP).

  • Familiarity with clinical development and real-world evidence (RWE) and how these influence scientific communication strategies.

  • Ability to navigate cross-functional partnerships with Clinical, Research/Translational Science, Biostatistics and executive teams.

  • 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.

  • Experience managing and mentoring teams of medical writers, communication specialists, or publication planners.

  • Ability to work in fast-paced, matrixed environments and lead cross-functional initiatives.

  • Proficiency in publication planning software (Datavision, PubStrat, etc.) and scientific engagement tools.

  • Strong project management skills to oversee multiple priorities, timelines, and stakeholders effectively.

Preferred Skills:

  • Experience in precision oncology and targeted therapies and gastrointestinal and/or thoracic cancers.

  • Previous leadership in launch planning and medical communications/publications strategy.

  • Expertise with digital tools and innovative solutions for medical communication.#LI-Hybrid  #LI-YG1

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