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Real World Evidence Rwe Jobs in Santa Clara, CA (NOW HIRING)

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Real World Evidence Rwe information

What is real world evidence (RWE)?

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.

How does a real world evidence (RWE) professional collaborate with cross-functional teams?

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 are the key skills and qualifications needed to thrive as a real world evidence (RWE) professional?

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.

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 are the most commonly searched types of Real World Evidence Rwe jobs in Santa Clara, CA?

The most popular types of Real World Evidence Rwe jobs in Santa Clara, CA are:

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For Real World Evidence Rwe jobs in Santa Clara, CA, the most frequently searched job titles are:

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What cities near Santa Clara, CA are hiring for Real World Evidence Rwe jobs?

Cities near Santa Clara, CA with the most Real World Evidence Rwe job openings:

Infographic showing various Real World Evidence Rwe job openings in Santa Clara, CA as of August 2026, with employment types broken down into 2% Internship, 90% Full Time, 5% Part Time, and 3% Contract. Highlights an 80% In-person, 3% Hybrid, and 17% Remote job distribution.

Senior Director, Real World Evidence Generation

Dompé farmaceutici S.p.A.

San Mateo, CA • On-site

$285 - $370/hr

Other

Medical, Retirement, PTO

Posted 18 days ago


Job description

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Senior Director, Real World Evidence Generation

Job Area: R&D/Medical

Job Category: Professionals

Job Site: Remote

Location: San Mateo, CA, US

Dompe is an Italian bio-pharmaceutical company that focuses on innovation, where a long tradition in the field of personal wellness goes hand-in-hand with a commitment to research and development to meet unsatisfied therapeutic needs.

Established in 1940 in Milan, Dompé has an industrial and biotech research hub in L’Aquila, in addition to branches in Europe (Barcelona, Berlin, Paris and Tirana). The company has approximately 900 employees. The US headquarters of Dompé are based in Boston (R&D) and in the San Francisco Bay Area (Commercial Operations).

Job Summary:

The Senior Director, Real World Evidence (RWE) leads the strategic design and execution of real-world data and evidence generation initiatives that support clinical value, market access, and lifecycle management goals. This individual is accountable for building a robust, compliant RWE agenda within the Evidence Generation team that complements clinical trial evidence across indications. The Senior Director partners closely with R&D, Market Access, and the Global Medical Leads to ensure evidence generation is scientifically rigorous and strategically relevant, and manages a team of RWE scientists responsible for translating real-world data into decision-ready insights.

Job Description: Integrated evidence strategy
  • Co-Own the Integrated Evidence Generation Plan (iEGP) across all Dompé indications—NAION, NK/PCED, AKC, oGVHD, and neurology pipeline—ensuring evidence priorities are strategically sequenced to support regulatory, payer, and scientific exchange goals
  • Partner with Global Medical Leads to translate indication-specific medical strategy into evidence priorities, identifying gaps between current data and the evidence needed for launch readiness, label expansion, or lifecycle management
  • Represent Evidence Generation in cross-functional governance forums including the Integrated Evidence Plan review, and serve as the senior MA voice in discussions with Clinical Development on trial-adjacent evidence needs
  • Maintain a forward-looking view of the competitive evidence landscape across indications, ensuring Dompé's evidence plan addresses emerging gaps or challenges
RWE strategy and study design
  • Provide strategic direction and senior oversight to the Associate Director of RWE & Epidemiology, ensuring the real-world evidence and epidemiology program is aligned to the iEGP and addresses payer, regulatory, and scientific exchange needs
  • Partner with Market Access and Commercial on the evidence requirements for HTA submissions and payer-facing evidence packages, ensuring the RWE and epidemiology program produces outputs that are credible, timely, and decision-grade
  • Represent RWE and epidemiology evidence in cross-functional medical strategy discussions, ensuring real-world data complements and contextualizes clinical trial data in the scientific narrative
Cross-functional alignment
  • Partner with R&D, Market Access, and Global Medical Leads to align evidence with payer and clinical needs
  • Support translation of RWE findings into publications, dossiers, and internal strategic recommendations
  • Manage relationships with external research partners, academic collaborators, and data vendors
Team and budget management
  • Build, mentor, and manage a team of RWE scientists and associate directors
  • Manage RWE budget and prioritization across therapeutic areas
  • Establish study prioritization criteria in partnership with senior Medical Affairs leadership
Qualifications: Required
  • PhD, PharmD, or equivalent in epidemiology, health outcomes, biostatistics, or related field
  • 10+ years of experience in real-world evidence, epidemiology, or outcomes research
  • Demonstrated experience designing and executing observational research
  • Strong understanding of real-world data sources (claims, EHR, registries)
  • Experience presenting evidence to internal and external stakeholders
Preferred
  • Experience in ophthalmology, immunology, or specialty care therapeutic areas
  • Publication record in peer-reviewed real-world evidence studies
  • Experience building an RWE function within a growing Medical Affairs organization
Competencies:
  • Methodological rigor: designs observational studies that hold up to scientific and regulatory scrutiny
  • Strategic prioritization: allocates limited evidence-generation resources to the studies with the highest clinical and business value
  • Stakeholder translation: converts complex real-world data into insights that HEOR, Market Access, and clinical teams can act on
  • External partnership: builds durable relationships with academic and data-vendor collaborators
  • Team development: coaches RWE scientists toward greater independence and strategic ownership
BENEFITS OF JOINING OUR TEAM
  • Comprehensive medical benefits: we value access to healthcare for our patients as well as our employees
  • Generous vacation / holiday time off: we care about our employees and encourage a balanced lifestyle
  • Competitive 401(K) matching

Base Salary: $285,000 - $370,000 a year

At Dompe, we offer an attractive compensation package to our team members. Any offer would include a competitive base salary (estimate shared above), incentive bonus, and benefits package customary to the position. Actual individual pay is determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.

We believe that the unique contributions of all employees create our success. To ensure that our products and culture continue to incorporate everyone’s perspectives and experience, we never discriminate based on race, religion, national origin, gender identity or expression, sexual orientation, age, or marital, veteran, or disability status. All your information will be kept confidential according to EEO guidelines.

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