Research Assistant (SRI) - Evaluative Clinical Sciences - Casual 2025-13081 (2025-13081)

Sunnybrook; Toronto; On-site; CAD 25,000 - 45,000; Part time

Job summary

An established industry player is seeking a Research Assistant to support evaluative clinical sciences. This casual role involves coordinating study activities, managing data collection, and ensuring compliance with regulatory processes. Ideal candidates will possess a background in science or healthcare, strong organizational skills, and proficiency in tools like Microsoft Office and REDCap. Join a dynamic team that values diversity and is committed to accessible employment practices, making a meaningful impact in clinical research.

Qualifications

• Post-secondary degree in science or healthcare or equivalent experience.
• Certification in clinical research and knowledge of regulatory processes.

Responsibilities

• Handle administrative tasks like preparing grant applications and enrolling patients.
• Monitor study progress and ensure protocols are followed.

Skills

Problem-solving

Communication

Organizational skills

Education

Post-secondary degree in science or healthcare

Certification in clinical research

Tools

Microsoft Office

REDCap

SAS

SPSS

Job description

Research Assistant (SRI) - Evaluative Clinical Sciences - Casual 2025-13081 (2025-13081)

Join to apply for the Research Assistant (SRI) - Evaluative Clinical Sciences - Casual 2025-13081 (2025-13081) role at Sunnybrook.

Responsibilities:

• Report to the Study PIs and work under the supervision of the Fellow, handling administrative tasks such as preparing grant applications, enrolling patients, and coordinating study activities.
• Monitor study progress to ensure protocols are followed and study tasks are completed.
• Maintain administrative logs, including study protocols, REB submissions, data review forms, and study visit records.
• Prepare and submit Regulatory Ethics applications and renewals.
• Coordinate data collection, source documentation, and data entry into study databases.
• Manage study visit schedules, assist with assessments, adverse event documentation, questionnaires, and sample collection.
• Participate in patient enrollment, randomization, and informed consent processes.

Qualifications:

• Post-secondary degree in science or healthcare, or equivalent experience.
• Certification in clinical research.
• Knowledge of regulatory processes and clinical source documentation.
• Proficiency in Microsoft Office and REDCap; experience with SAS or SPSS is a plus.
• Strong problem-solving, communication, and organizational skills.
• Ability to work independently in a fast-paced environment.
• Respectful, responsible, with high integrity and confidentiality.

Details:

• Casual position, approximately 5-10 hours/week.
• To apply, send a letter of interest and an updated resume.
• We value diversity and are committed to accessible employment practices.