Clinical Lab & Research Assistant - Toronto & Scarborough
On-siteToronto, Ontario, Canada
Job Summary
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 while entering and maintaining accurate data in electronic data capture (EDC) systems. Prepare regulatory binders for IRB submissions and coordinate subject visits, phlebotomy, lab work, and investigational product dispensing. Communicate with sponsors, CROs, and IRBs regarding protocol queries and ongoing monitoring, and assist in preparation for sponsor monitoring visits and regulatory audits. Maintain investigational product accountability logs under PI supervision. Requires Bachelor's degree in life sciences, phlebotomy certification, and familiarity with GCP and EDC systems.
Required Qualifications
- 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
- Exceptional organizational skills and attention to detail
- Strong written and verbal communication skills
- Ability to manage competing priorities in a fast-paced environment
Desired Qualifications
- Familiarity with GCP, ICH guidelines, and FDA & HC regulations is a strong plus
- Experience with EDC systems (Medidata Rave, INFORM, Veeva Vault) a plus
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