Clinical Research Associate (CRA) – Oncology | Canada
- Toronto, ON
- On-site
- Posted Nov 4, 2026
- 1 position
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- Employment type
- Full-time
- Experience level
- Mid-level · 2+ years
- Minimum education
- Bachelor’s degree
- Posting language
- English
- Working hours
- 40 hours per week
- Seniority
- Entry level
- Application method
- Apply on LinkedIn (LinkedIn sign-in required)
Job summary
Serve as the primary communication link between the study team and site team under the direction of the Clinical Trial Leader. Conduct clinical research activities in accordance with customer specifications, company standards, and applicable regulations.
Job details
About Scimega Scimega is a specialized CRO skilled in collaborative vendor teaming with 29 years unparalleled Canadian oncology experience, 150+ successful oncology clinical trials - never rescued by another CRO. Our business model and experienced team of oncology experts effectively support small and mid-size biotechs in successful execution of clinical trials at Canadian Cancer Research Centers. Clinical Research Associate (CRA) Under the direction of Clinical Trial Leader (CTL) and in accordance with customer specifications/values, Scimega’s corporate standards, and applicable regulations, the Clinical Research Associate (CRA) is the main line of communication between the study team and the site team. Required Qualifications: Education: Bachelor’s Degree in a Health Science field or registered nurse Experience: Minimum 2 years’ experience as a CRA or as a study coordinator, preferably in the field of oncology. Other: Excellent knowledge in the field of oncology, very good knowledge of the Good Clinical Practices. Languages spoken and written: French and English if based in the province of Quebec, English if based in any other province. Ability to travel to domestic and international destinations What Our Employees Say… “I work with highly intelligent people who CARE to get their job done well, and dedicate themselves to our team (as opposed to punching in and out every day). We work on some of the most exciting oncology projects in North America, and I am given the opportunity to grow and contribute to the team's success at every turn. Scimega Employee, Toronto, Canada Please visit our website for more information: https://scimega.com/ You may send your candidature to careers@scimega.com
What you’ll do
Serve as the primary communication link between the study team and site team under the direction of the Clinical Trial Leader. Conduct clinical research activities in accordance with customer specifications, company standards, and applicable regulations.
Requirements
Requires a bachelor's degree in a health science field or registered nurse qualification, and at least two years of experience as a Clinical Research Associate or study coordinator; oncology experience is preferred. Candidates need excellent oncology knowledge, very good knowledge of Good Clinical Practice, and English; French is also required for roles based in Quebec.
Listed skills
- Site Communication · Preferred
- Regulatory Compliance · Preferred
- French · Preferred
- English · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Oncology
- Clinical Research
- Clinical Trial Monitoring
- Good Clinical Practice
- Site Communication
- Study Coordination
- Regulatory Compliance
- Domestic And International Travel
- French
- English
Job areas
- Healthcare
- Science & Research