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, 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)

Familiarity with GCP, ICH guidelines, and FDA & HC regulations is a robust 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

📌 Clinical Research Assistant (Toronto)
🏢 ClinSurge Research
📍 Toronto