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Internship Real World Evidence Rwe Jobs in Quebec

... re a world leader in recreational vehicles and boats, creating innovative ways to move on snow ... You'll have the opportunity to work on stimulating projects and make a real impact. At BRP, you'll ...

... re a world leader in recreational vehicles and boats, creating innovative ways to move on snow ... You'll have the opportunity to work on stimulating projects and make a real impact. At BRP, you'll ...

... re a world leader in recreational vehicles and boats, creating innovative ways to move on snow ... You'll have the opportunity to work on stimulating projects and make a real impact. At BRP, you'll ...

This internship in automn 2026 will allow you to develop a solid understanding of real world civil construction activities and the specific challenges of renewable energy projects. This role is ...

This internship in automn 2026 will allow you to develop a solid understanding of real world civil construction activities and the specific challenges of renewable energy projects. This role is ...

This internship in automn 2026 will allow you to develop a solid understanding of real world civil construction activities and the specific challenges of renewable energy projects. This role is ...

About the role We're seeking motivated interns to contribute to the development of AI systems ... Passion for applying ML research to real-world problems. Nice to have: * Authorship of a ...

... real-world prediction and natural language processing problems. * Experience integrating large ... or internship-are subject to a criminal background check. Positions that involve access to ...

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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, 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 job categories do people searching Internship Real World Evidence Rwe jobs in Quebec look for? The top searched job categories for Internship Real World Evidence Rwe jobs in Quebec are:
What cities in Quebec are hiring for Internship Real World Evidence Rwe jobs? Cities in Quebec with the most Internship Real World Evidence Rwe job openings:
Associate Director, Epidemiology (HPV)

Associate Director, Epidemiology (HPV)

GlaxoSmithKline

Montreal, QC • Hybrid

Full-time

Posted 6 days ago


GlaxoSmithKline rating

8.9

Company rating: 8.9 out of 10

Based on 19 frontline employees who took The Breakroom Quiz

8th of 71 rated pharmaceutical


Job description

Business Introduction
At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people's lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients' needs and have the highest probability of success. We're uniting science, technology, and talent to get ahead of disease together.
Find out more:
Our approach to R&D

The Associate Director, Epidemiology (HPV) will provide scientific leadership in disease epidemiology, leveraging real-world data (RWD), cutting-edge methods, and technology across medicine and vaccine development. The role aims to generate credible and actionable real-world evidence (RWE) to improve patient outcomes, aligning epidemiology programs with broader asset/disease strategies to deliver new medicines and vaccines efficiently and effectively.

Join us to grow your skills, influence decisions that affect patients, and contribute to GSK's mission of uniting science, technology and talent to get ahead of disease together.
Responsibilities:
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Accountable for the epidemiology program for at least one asset or disease area, including proposing and negotiating program content and budget with matrix leaders. This includes developing a Global Epidemiology Plan and may include leading a cross-functional team.

  • Provide expert epidemiological insights to asset matrix teams (e.g., Clinical Development Team, Safety Review Team, Medicine/Vaccine Development Team).

  • Lead complex epidemiological studies and negotiate new partnerships with oversight from senior staff.

  • Identify new vendors, tools, and data sources to deliver innovative epidemiology solutions for assets or disease areas.

  • Contribute to strategic initiatives on the role of epidemiology at the departmental or R&D level.

  • Represent GSK in scientific interactions with internal governance bodies, external regulators, and at international conferences.

  • Plan and coordinate scientific dissemination of epidemiology data, including authoring regulatory documents, peer-reviewed publications, and presentations at national and international meetings.

  • Partner with external groups conducting epidemiological studies globally and manage external collaborations.


Why You?


Basic Qualifications:
We are seeking professionals with the following required skills and qualifications to help us achieve our goals.

  • Master's degree in Epidemiology, Public Health, Biostatistics, or a related quantitative discipline.

  • Epidemiological experience and ability to influence key internal (matrix leaders) and external (e.g. regulators) stakeholders.

  • Experience applying epidemiologic methods inpharmacoepidemiology,clinical development, or outcomes research.

  • Experience designing and delivering observational and database studies, including protocol development and analysis oversight.

  • Experience working in a matrix environment and influencing multidisciplinary teams.

  • Experience providing the delivery of increasingly complex epidemiological studies, including regulatory requirements.

  • Experience applying epidemiology methods and study design knowledge in execution of their work (e.g. post-approval studies).

  • Experience working with external regulatory requirements and scientific landscape around RWE.


Preferred Qualifications:
If you have the following characteristics, it would be a plus.

  • Doctoral degree (PhD, ScD, DrPH) in Epidemiology, Public Health, Biostatistics, or a related quantitative discipline.

  • 1+ years in the pharmaceutical industry or equivalent experience in an academic or government setting.

  • Experience using epidemiology background for HPV studies.

  • Experience in the pharmaceutical or biotechnology industry supporting regulatory submissions or post-authorization commitments.

  • Track record using multiple real-world data sources (claims, electronic health records, registries) and familiarity with data linkage.

  • Experience with advanced quantitative methods such as propensity scores, target trial emulation, or causal inference approaches.

  • Familiarity with safety signal evaluation and background rate estimation for risk assessment.

  • Active participation in scientific networks or professional societies and a record of peer-reviewed publications.

  • Prior experience presenting to regulators, advisory boards or scientific conferences.

  • Highly proficient written, verbal, and listening skills.


Working Model
This role is expected to be hybrid, with a mix of remote and 3 days a week on-site work.

#GSK-LI

In compliance with Ontario's provincial pay transparency legislation, this job posting includes a salary range to support equitable and informed hiring practices. The annual compensation for this role is CAD129,000 to CAD179,000 , determined based on experience, qualifications, and internal equity. GSK is dedicated to promoting transparency and fairness throughout our recruitment process.Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process.

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at -usrecruitment.adjustments@gsk.com

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/


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About GlaxoSmithKline

Sourced by ZipRecruiter

GlaxoSmithKline is a globally recognized pharmaceutical and healthcare company based in Philadelphia, PA, USA. Originated from a merger between Glaxo Wellcome and SmithKline Beecham in 2000, the company excels in the pharmaceutical industry and holds a leading position in making medicines, vaccines, and consumer healthcare products. GSK's mission is to improve the quality of human life by enabling people to do more, feel better, and live longer. They adhere to core values of transparency, integrity, respect for people, and patient-focus, reflecting in their endeavors to conduct research and deliver innovative healthcare solutions to patients and consumers worldwide.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

Philadelphia, PA, US