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Internship Real World Evidence Rwe Jobs in San Ramon, CA

... 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 ...

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 ...

... 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 ...

... 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 ...

... 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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Internship Real World Evidence Rwe information

See San Ramon, CA salary details

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How much do internship real world evidence rwe jobs pay per hour?

As of Jul 1, 2026, the average hourly pay for internship real world evidence rwe in San Ramon, CA is $17.37, according to ZipRecruiter salary data. Most workers in this role earn between $13.99 and $19.62 per hour, depending on experience, location, and employer.

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

To thrive as an Internship Real World Evidence (RWE) professional, you need a solid background in life sciences, epidemiology, or statistics, often supported by progress toward a relevant degree. Familiarity with data analysis tools like SAS, R, or Python, and experience with healthcare databases or real-world data systems, are typically required. Strong analytical thinking, attention to detail, and collaborative communication skills help interns excel in cross-functional teams and data-driven projects. These competencies are crucial for generating robust, actionable insights from real-world data to inform healthcare decisions and policy.

What is an Internship in Real World Evidence (RWE)?

An Internship in Real World Evidence (RWE) offers students or recent graduates hands-on experience in collecting and analyzing data from real-world sources, such as electronic health records, insurance claims, and patient registries. RWE is used in the pharmaceutical and healthcare industries to evaluate the effectiveness, safety, and value of medical treatments outside controlled clinical trials. Interns may support research studies, help interpret data, and contribute to reports that inform decision-making for healthcare providers and regulators. This type of internship is ideal for those interested in data analysis, public health, and evidence-based medicine.

What types of projects do interns typically work on in a Real World Evidence (RWE) internship?

As an RWE intern, you can expect to contribute to projects involving the collection, analysis, and interpretation of real-world healthcare data, such as electronic health records, claims data, or patient registries. Common responsibilities include supporting data cleaning, conducting literature reviews, assisting with statistical analyses, and preparing reports or presentations for internal teams. You will often collaborate with cross-functional teams including epidemiologists, data scientists, and medical affairs professionals, which provides excellent exposure to various aspects of the pharmaceutical or healthcare industry.

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

AspectInternship Real World Evidence RweData Analyst
Required CredentialsTypically pursuing or recent graduate in healthcare, life sciences, or related fieldsBachelor's degree in statistics, mathematics, computer science, or related fields
Work EnvironmentHealthcare or pharmaceutical companies, research organizations, or academic institutionsVarious industries including finance, healthcare, marketing, and technology
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare sectors for evidence generationWidely used across multiple industries for data analysis and reporting

While both roles involve working with data, an Internship Real World Evidence Rwe focuses on analyzing real-world healthcare data to generate evidence for medical decisions, often within healthcare or pharma settings. A Data Analyst has a broader scope, working with various data types across industries to interpret and visualize data for business insights.

What are popular job titles related to Internship Real World Evidence Rwe jobs in San Ramon, CA? For Internship Real World Evidence Rwe jobs in San Ramon, CA, the most frequently searched job titles are:
What cities near San Ramon, CA are hiring for Internship Real World Evidence Rwe jobs? Cities near San Ramon, CA with the most Internship Real World Evidence Rwe job openings:
Senior Scientist, Scientific Affairs

Senior Scientist, Scientific Affairs

Recor Medical

Palo Alto, CA

$166K - $181K/yr

Full-time

Posted 5 days ago


Job description

At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our Paradise uRDN System, we're on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe.

Position Summary
We are seeking an execution-focused scientific leader to drive the management of global External Research programs, including Investigator-Sponsored Research (ISR). This role owns planning, execution, and delivery of multiple concurrent clinical and scientific initiatives in close partnership with leadership, physicians, and cross-functional teams.
The Senior Scientist will serve as a hands-on program leader, ensuring timelines, budgets, and quality standards are met while proactively managing risks and operational complexity. The role requires strong scientific fluency in interpreting clinical data, guide evidence generation, and communication that support product differentiation and clinical adoption.
The ideal candidate thrives in fast-paced environments, takes initiative, and excels at managing competing priorities while driving programs from concept through completion.


Key Responsibilities
Scientific Affairs & Physician Engagement
Lead development of abstracts, publications, presentations, and scientific materials
Lead or support physician interactions, advisory boards, and working groups to advance study objectives and scientific understanding


Scientific Strategy & Evidence Generation
Contribute to and influence the development and execution of the Scientific Affairs and evidence-generation strategy aligned with organizational and product priorities
Identify evidence gaps and help prioritize clinical, real-world evidence (RWE), and investigator-led research initiatives


Cross-Functional Program Management
Lead external research across regions to ensure alignment on clinical and scientific objectives
Track and communicate program status, milestones, and outcomes to senior leadership


Clinical Program Management
Serve as lead program manager and primary point of accountability for assigned global clinical studies from initiation through close-out
Develop and maintain integrated project plans, timelines, budgets, and resourcing strategies
Ensure study outputs are actionable and aligned with downstream publication, regulatory, and commercialization needs
Ensure compliance with ICH-GCP, FDA, EU MDR, and applicable global regulatory standards
Support inspection and audit readiness (FDA, notified bodies, internal audits)


Vendor, Site & Financial Oversight
Oversee study budgets, tracking, and financial performance
Provide input into contracts, payments, and site engagement strategies


Team & Leadership Contributions
Mentor junior team members and contribute to a high-performing, collaborative culture
Drive accountability, ownership, and a bias toward action across teams
1049 Elwell Court, Palo Alto, CA 94303 www.recormedical.com
Contribute to building scalable Scientific Affairs capabilities, including frameworks for evidence generation, external research governance, and best practices


Qualifications
Experience
12+ years (Bachelor's), 8+ years (Master's), or 5+ years (PhD) in MedTech, Biotech, Pharma, or related industry
Demonstrated success leading global clinical programs and external research initiatives


Core Capabilities
Ability to distill and communicate complex clinical data to diverse stakeholders
Strong expertise in clinical study execution and regulatory frameworks (ICH-GCP required)
Experience working with KOLs, investigators, and advisory boards
Proven ability to manage cross-functional programs and external partners (CROs/vendors)
Scientific writing, data interpretation, and publication experience; working knowledge of statistics required


Leadership & Execution Skills
Excellent communication, influencing, and stakeholder management skills
Strong problem-solving ability in fast-paced, ambiguous environments
Highly organized, proactive, and results-oriented


Other
Therapeutic area experience (e.g., hypertension, cardiology, vascular physiology)
Proficiency in Microsoft Office (Word, Excel, PowerPoint, Outlook)

Salary range: $166,954 - $181,000 (Commensurate with experience, skills, education and training)

The successful candidate's starting base pay will be determined based on job-related skills, experience, qualifications, work location and market conditions. The expected base pay range for this role may be modified based on market conditions.

Equal Employment Opportunity
At Recor Medical, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.

Pre-Employment Requirement

At Recor Medical, patient safety and compliance are at the heart of everything we do. To support these standards, employment for all field-based roles is contingent upon successfully completing a pre-employment background check and/or drug screen. These steps help ensure we bring the highest level of integrity and accountability to the physicians and patients we serve.

Radiation Safety Requirement

Certain field-based roles at Recor Medical require work in environments where radiation sources (e.g., x-ray equipment) are in use. Employees in these roles will be issued a personal dosimetry badge to monitor occupational exposure and are required to wear it in accordance with company policy and applicable regulatory standards. This program is designed to ensure compliance with federal and state regulations and to maintain radiation exposure at levels that are As Low As Reasonably Achievable (ALARA). Additional guidance and protective equipment, as necessary, will be provided as part of onboarding and ongoing safety training.

Respecting your privacy is an essential part of the Company's privacy program and we are committed to the proper handling of Personal Information collected or processed in connection with an Applicant's application for employment, a Contract Worker's work, or a Former Employee's employment at Recor. Refer to our Applicant, Contract Worker & Former Employee Privacy Policy for more detail information.