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Internship Real World Evidence Rwe Jobs in California

Dexcom, Inc.

Chief Medical Officer

San Diego, CA · On-site

Own the evidence roadmap and ensure the right mix of clinical studies and real-world evidence supports adoption, guidelines, and growth. * Lead HEOR and RWE efforts, producing payer-ready evidence ...

RXinsider LTD.

Chief Medical Officer

San Diego, CA · On-site

$231.90 - $481.50/hr

Own the evidence roadmap and ensure the right mix of clinical studies and real-world evidence supports adoption, guidelines, and growth. * Lead HEOR and RWE efforts, producing payer-ready evidence ...

Dexcom

Chief Medical Officer

San Diego, CA · On-site

Own the evidence roadmap and ensure the right mix of clinical studies and real-world evidence supports adoption, guidelines, and growth. * Lead HEOR and RWE efforts, producing payer-ready evidence ...

Travere Therapeutics

Senior Biostatistician

San Diego, CA · On-site

$116 - $151/hr

... Real World Evidence (RWE), and Market Access activities in support of drug development and commercialization. This role contributes to statistical aspects of assigned studies or projects to ensure ...

Travere

Senior Biostatistician

San Diego, CA · On-site +1

... Real World Evidence (RWE), and Market Access activities in support of drug development and commercialization. This role contributes to statistical aspects of assigned studies or projects to ensure ...

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Internship Real World Evidence Rwe information

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

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.

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Internship Real World Evidence Rwe jobs near you

Senior Principal Biostatistician (Epidemiology)

Edwards Lifesciences Corporation

Irvine, CA • On-site

Full-time

Posted 10 days ago

Edwards Lifesciences rating

8.3

Company rating: 8.3 out of 10

Based on 30 frontline employees who took The Breakroom Quiz

66th of 537 rated manufacturers

Job description

Patients are at the heart of everything we do. As part of our Medical Affairs team, you'll foster internal and external collaboration to generate and disseminate evidence-based clinical practices to help impact patient lives and advance the quality of care. Your scientific curiosity and passion for patients will help us grow our reach and develop innovative solutions for people fighting cardiovascular disease.
Patients with mitral and tricuspid heart valve disease often have complex conditions with limited treatment options. Our Transcatheter Mitral and Tricuspid Therapies (TMTT) business unit is boldly pursuing an innovative portfolio of technologies to address a patient's unmet clinical needs. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.
The Senior Principal Biostatistician (Epidemiology) will represent the Biostatistics department on all aspects of the clinical development process, ranging from clinical trial designs to regulatory submissions while applying scientific rigor to statistical methods and interpretation of results and also advise on the conduct of clinical studies, database development and data quality assurance with the analysis of clinical endpoints in mind.
How you will make an impact:
  • Lead end-to-end evidence strategies, designing observational studies, interventional trials, and real-world evidence (RWE) programs to support pipeline and on-market products
  • Build economic models (cost-effectiveness, budget impact) to clearly communicate the clinical, and economic value of Edwards products
  • Statistical lead on multiple clinical trials, lead the coordination of analyses for study report and other documents and provide programming and validation support of these analyses
  • Collaborate with cross-functional partners and external analysts in the execution of studies and implementation of field-based, customer-focused initiatives and partnerships (e.g., models, presentations, publications, formulary/regulatory dossiers).
  • Represent Biostatistics on multiple project/study teams and coordinate/communicate with management and other team members regarding project/study status and timeline update
  • Provide statistical expertise and guidance to internal and external stakeholders on ad hoc data analysis requests and publication/presentation efforts related to the project team
  • Research and recommend novel statistical methodology and/or approaches
  • Contribute to the improvement, standardization, and globalization of Biostatistics processes and procedures, including the development of Biostatistics Standard Operating Procedures (SOPs) and Work Instruction Manuals (WIMs)
  • Lead the efforts of data analysis for data monitoring committee as needed
  • Mentor junior statisticians and work with management in resource allocation and budget/timeline development activities

What you'll need (Required):
  • Bachelor's Degree in Statistics, Biostatistics, or related field, 8 years of previous analytical experience in clinical trials or
  • Master's Degree or equivalent in Statistics, Biostatistics, or related field, 7 years of previous analytical experience in clinical trials or
  • Ph.D. or equivalent in Statistics, Biostatistics, or related field , 4 years of experience

What else we look for (Preferred):
  • Medical device industry experience strongly preferred, including statistical support for clinical studies, real-world evidence, and regulatory submissions.
  • Deep knowledge of outcomes research and RWE methodologies (study design, statistics, data sources, and implementation)
  • Deep knowledge of observational study methods, causal inference, economic model (cost-effectiveness), epidemiology
  • Proven experience managing vendors, budgets, and building productive partnerships with internal stakeholders and external experts/KOLs
  • Demonstrated leadership in matrixed environments, including the ability to direct work across functions to deliver shared objectives
  • Proven expertise in SAS required; experience using other software packages (e.g., R, S-Plus) preferred Proven expertise in MS Office Suite including Word, PowerPoint, Access, and Excel
  • Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives
  • Keeps abreast of new developments in statistics and regulatory guidance
  • Expert understanding and knowledge in statistical methodologies related to clinical trial designs, statistical modeling and data analyses
  • Expert understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device research setting
  • Excellent problem-solving, organizational, analytical and critical thinking skills
  • Strong leadership skills and ability to influence change
  • Ability to provide training and coaching to lower level employees
  • Experience in facilitating change, including collaboration with management and executive stakeholders

Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.
For California, the base pay range for this position is $151,000 - $215,000 (highly experienced).
The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.
Edwards is an Equal Opportunity/Affirmative Action employer including protected Veterans and individuals with disabilities.

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About Edwards Lifesciences

Sourced by ZipRecruiter

Edwards Lifesciences is the global leader in patient-focused medical innovations for structural heart disease, as well as critical care and surgical monitoring. Driven by a passion to help patients, the company collaborates with the world's leading clinicians and researchers to address unmet healthcare needs, working to improve patient outcomes and enhance lives. Headquartered in Irvine, California, Edwards Lifesciences has extensive operations in North America, Europe, Japan, Latin America and Asia and currently employs over 15,000 individuals worldwide. For us, helping patients is not a slogan - it's our life's work. From developing devices that replace or repair a diseased heart valve to creating new technologies that monitor vital signs in the critical care setting, we focus on helping patients regain and improve the quality of their life.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Irvine, CA, US

Year founded

1958

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