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Internship Real World Evidence Rwe Jobs in Toronto, ON

... drive" safely in the real world, Waabi is bringing the promise of self-driving closer to ... Application Instructions: - To be considered for an internship/co-op, please add your most up to ...

We specialize in advising clients on medical affairs, clinical studies, real-world evidence, marketing, advocacy, and communications, all underpinned by insights and creative strategy. AXON has an ...

Join our firm for an internship journey where you'll dive into real-world project work, learn from industry leaders and fully immerse yourself in the CRB employee experience. This program is more ...

You will have the opportunity to make a real impact with an organization that truly cares, from ... of the world, our perspective and our approach. * On-the-job training, with opportunities to ...

You will have the opportunity to make a real impact with an organization that truly cares, from ... of the world, our perspective and our approach. * On-the-job training, with opportunities to ...

You will have the opportunity to make a real impact with an organization that truly cares, from ... of the world, our perspective and our approach. * On-the-job training, with opportunities to ...

You will have the opportunity to make a real impact with an organization that truly cares, from ... of the world, our perspective and our approach. * On-the-job training, with opportunities to ...

This role does not conduct real-world evidence studies. About YOU * Advanced degree (Master's or PhD) in Epidemiology, Biostatistics, Health Informatics, Health Economics, Pharmacoepidemiology, or a ...

This role does not conduct real-world evidence studies. About YOU * Advanced degree (Master's or PhD) in Epidemiology, Biostatistics, Health Informatics, Health Economics, Pharmacoepidemiology, or a ...

This role does not conduct real-world evidence studies. About YOU * Advanced degree (Master's or PhD) in Epidemiology, Biostatistics, Health Informatics, Health Economics, Pharmacoepidemiology, or a ...

Showing results 21-40

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.

What are popular job titles related to Internship Real World Evidence Rwe jobs in Toronto, ON? For Internship Real World Evidence Rwe jobs in Toronto, ON, the most frequently searched job titles are:
What job categories do people searching Internship Real World Evidence Rwe jobs in Toronto, ON look for? The top searched job categories for Internship Real World Evidence Rwe jobs in Toronto, ON are:
Infographic showing various Internship Real World Evidence Rwe job openings in Toronto, ON as of August 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person job distribution.

Clinical Program Manager

Science&Humans

Mississauga, ON โ€ข On-site

Full-time

Posted 17 days ago


Job description

Salary: $ 90,000 -110,000

Clinical Program Manager

Reports to: Chief Product Officer

Type: Individual Contributor

Location: Greater Toronto Area (GTA) Hybrid, 3 days onsite / 2 days remote


About Science & Humans

Science & Humans (S&H) is a health tech company bridging the gap between hormone health and real-world care. Our mission is to deliver personalized, technology-enabled solutions that empower individuals and practitioners to manage hormone and longevity-related conditions. Through e-commerce, telehealth, AI-driven clinical decision support, and advanced analytics, we're transforming traditional healthcare into proactive, personalized care, at scale.


About the Role

We are seeking a Clinical Program Manager to own the product roadmap for our Women's Health portfolio. This is an individual contributor role reporting directly to the Chief Product Officer, ideal for someone who combines rigorous clinical research training with a passion for building patient- and clinician-facing digital health products.

You'll sit at the intersection of clinical science, technology, and functional medicine, translating clinical evidence and patient needs into product requirements that our engineering and design teams can build against. This role suits a scientist-turned-product-thinker who wants to see their clinical expertise shape real-world digital health tools.


Key Responsibilities

  • Own and drive the end-to-end product roadmap for the Women's Health / Telehealth product line, from discovery through launch and iteration.
  • Translate clinical evidence, trial data, and regulatory considerations into clear product requirements and user stories.
  • Partner closely with clinical teams and functional medicine practitioners to ensure product decisions are grounded in sound clinical rationale and patient safety.
  • Collaborate with engineering/technology teams to scope, prioritize, and deliver features across web and mobile platforms.
  • Define and track success metrics for clinical efficacy, patient engagement, and product adoption.
  • Support regulatory and quality documentation as needed for Software as a Medical Device (SaMD) or telehealth compliance requirements.
  • Conduct competitive and clinical literature research to identify emerging opportunities in women's health and remote care.
  • Act as the clinical/product bridge in cross-functional planning, ensuring stakeholder alignment across technical, clinical, and business teams.


Qualifications

Required

  • PhD required in a clinical research, biology, or related life sciences discipline.
  • Hands-on clinical trial experience (e.g., trial design, data collection, protocol execution, or clinical research coordination) this may come from doctoral research, postdoctoral work, or prior industry roles.
  • Strong written and verbal communication skills, with the ability to translate complex clinical concepts for non-clinical audiences (engineers, designers, business stakeholders).
  • Comfort working in a fast-paced, hybrid, cross-functional environment.

Experience Level

This role is designed to be accessible to candidates early in their product career but strong in clinical grounding:

  • New PhD graduates or those with 12 years of post-PhD experience are encouraged to apply.
  • Prior formal product management experience is not required, clinical research rigor and domain expertise are weighted more heavily than traditional PM tenure.
  • 12 years of exposure to digital health, telehealth, or health-tech products (internship, research, consulting, or industry) is preferred but not mandatory; candidates without this can demonstrate transferable skills through clinical trial project management, data analysis, or research translation work.

Preferred

  • Familiarity with product types such as patient-facing apps, clinician-facing tools, Software as a Medical Device (SaMD), remote patient monitoring platforms, or EHR-adjacent systems.
  • Background or strong interest in women's health, reproductive health, or telehealth.
  • Exposure to functional or integrative medicine approaches.
  • Understanding of health data privacy and regulatory basics (e.g., PHIPA, HIPAA, Health).


Cross-Functional Partners

  • Technology / Engineering
  • Clinical Team
  • Functional Medicine practitioners
  • Design / UX
  • Regulatory & Quality (as needed)


Why Join Us

This is a rare opportunity for a clinically-trained scientist to step directly into product leadership on a mission-driven women's health platform, shaping the roadmap, not just executing on it, with direct visibility to the Chief Product Officer.


We use automated and AI software to help score and rank applicant qualifications. A human recruiter reviews all candidate files before any interview or hiring choice.