Clinical Research Associate (CRA) – Oncology | Canada

Job summary

Serve as the main point of communication 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 main point of communication 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 CRA or study coordinator, preferably in oncology. Candidates should have excellent oncology knowledge, very good knowledge of Good Clinical Practices, the required language proficiency for their province, and the ability to travel domestically and internationally.

Listed skills

• Site Communication · Preferred
• Regulatory Compliance · Preferred

Other relevant skills

Identified from the job description. Confirm important requirements above.

• Oncology
• Good Clinical Practices
• Clinical Trial Monitoring
• Clinical Research
• Site Communication
• Study Coordination
• Regulatory Compliance
• Travel

Job areas

• Healthcare
• Science & Research

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