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Internship Clinical Research Informatics Jobs in Toronto, ON

Mercor

Pharmacy Expert - Lexidrug Specialist

Toronto, ON · Remote

CA$75 - CA$120/hr

About the job Mercor connects elite creative and technical talent with leading AI research labs ... Judge completeness of the clinical picture, ensuring all active meds, labs, and comorbidities are ...

Mercor

Pharmacy Expert - Lexidrug Specialist

Toronto, ON · Remote

CA$75 - CA$120/hr

About the job Mercor connects elite creative and technical talent with leading AI research labs ... Judge completeness of the clinical picture, ensuring all active meds, labs, and comorbidities are ...

Humber River Health

Registered Dietitian

Toronto, ON · On-site

CA$41.68 - CA$53.28/hr

Clinical Excellence, Optimizing Care through Technology and Community Connection frame our Research ... Completion of an internship program and a member (or eligibility to become a member) of the ...

Humber River Health

Registered Dietitian

Toronto, ON · On-site

CA$41.68 - CA$53.28/hr

Clinical Excellence, Optimizing Care through Technology and Community Connection frame our Research ... Completion of an internship program and a member (or eligibility to become a member) of the ...

Roche

Medical Strategy Intern

Mississauga, ON · Hybrid

Conduct desktop market research on therapeutic trends, clinical trials, and healthcare ecosystem ... Term & Location: 12-month full-time internship starting January 2027 in Mississauga, ON (Hybrid ...

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Internship Clinical Research Informatics information

What is an internship in clinical research informatics?

An Internship in Clinical Research Informatics is a temporary position designed for students or recent graduates to gain hands-on experience in managing and analyzing data in clinical research settings. Interns typically work alongside experienced informaticians and researchers to support clinical trials, data management, and the development of health information systems. The role helps interns develop skills in data analysis, electronic health records, and research methodology. It is an ideal starting point for those interested in the intersection of healthcare, research, and information technology.

What types of projects or tasks can I expect to work on during an internship in clinical research informatics?

As a Clinical Research Informatics intern, you may be involved in tasks such as managing and analyzing clinical trial data, assisting with the development or optimization of electronic data capture systems, and supporting data quality assurance processes. Interns often collaborate closely with clinical research coordinators, data managers, and IT teams to ensure data integrity and regulatory compliance. You might also contribute to the design of study databases, help generate reports for ongoing studies, and participate in team meetings to discuss project progress. This role provides valuable exposure to both technical and clinical aspects of research, offering a strong foundation for future career growth in informatics or clinical research.

What are the key skills and qualifications needed to thrive as an intern in clinical research informatics?

To thrive in an Internship Clinical Research Informatics role, candidates typically need a background in life sciences or health informatics, basic understanding of clinical research methodologies, and strong analytical skills. Familiarity with data management tools, electronic data capture (EDC) systems, and statistical software like SAS or R is often expected. Attention to detail, effective communication, and a willingness to learn are valuable soft skills that help interns stand out. These skills are crucial for ensuring accurate data handling, supporting research teams, and contributing to successful clinical research outcomes.

What is the difference between Internship Clinical Research Informatics vs Clinical Data Analyst?

AspectInternship Clinical Research InformaticsClinical Data Analyst
Required CredentialsTypically pursuing or recent graduate in health informatics, life sciences, or related fieldsBachelor's or master's in health informatics, data science, or related areas
Work EnvironmentInternship setting within research institutions, hospitals, or pharmaceutical companiesHealthcare organizations, research institutions, or data-focused teams
Employer & Industry UsageUsed in academic, clinical research, and pharmaceutical sectors for training and entry-level rolesCommon in healthcare and research for analyzing clinical data and supporting decision-making

Internship Clinical Research Informatics focuses on training and gaining experience in managing clinical data and informatics systems, often as a stepping stone into the industry. Clinical Data Analysts primarily analyze and interpret clinical data to support research and healthcare decisions. Both roles involve working with health data but differ in experience level and focus.

Internship Clinical Research Informatics jobs near you
Infographic showing various Internship Clinical Research Informatics job openings in Toronto, ON as of July 2026, with employment types broken down into 2% As Needed, 75% Full Time, 16% Part Time, and 7% Contract. Highlights an 92% Physical, 4% Hybrid, and 4% Remote job distribution.

Clinical Lab & Research Assistant - Toronto & Scarborough

Toronto, ON • On-site

ClinSurge Research
See more jobs at ClinSurge Researchexternal

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Clinical Research Assistant - on-site role

About ClinSurge Research 

ClinSurge Research is a dynamic clinical research organization dedicated to advancing medical science through rigorous, patient-centered trials. We partner with leading sponsors, and healthcare systems to bring breakthrough therapies to the patients who need them most. Join a team that moves fast, works with purpose, and takes pride in scientific integrity.

Role overview

We are seeking a detail-oriented and motivated Clinical Research Assistant to support our growing portfolio of clinical trials. You will work closely with Principal Investigators, Study Coordinators, and sponsors to ensure smooth trial execution—from patient recruitment through data lock.

What you'll do
  • Assist with patient recruitment, screening, and enrollment activities across multiple active protocols
  • Collect, record, and verify source data in compliance with GCP guidelines and study protocols
  • Enter and maintain accurate data in electronic data capture (EDC) systems
  • Prepare, organize, and maintain regulatory binders (IRB submissions, essential documents)
  • Coordinate and schedule subject visits, phlebotomy, lab work, and investigational product dispensing
  • Communicate with sponsors, CROs, and IRBs regarding protocol queries and ongoing monitoring
  • Assist in preparation for sponsor monitoring visits and regulatory audits
  • Maintain investigational product accountability logs under PI supervision
What we're looking for
  • Bachelor's degree in life sciences, public health, or a related field
  • 0–2 years of experience in a clinical research or healthcare setting (internships welcome)
  • Phlebotomy certification and with experience and proficiency
  • Familiarity with GCP, ICH guidelines, and FDA & HC regulations is a strong plus
  • Experience with EDC systems (Medidata Rave, INFORM, Veeva Vault) a plus
  • Exceptional organizational skills and attention to detail
  • Strong written and verbal communication skills
  • Ability to manage competing priorities in a fast-paced environment

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