Clinical Research Assistant - Lab Technician

Mississauga, ONOnsiteFull TimePosted 17 days ago

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Required skills

GCP
ICH guidelines
FDA regulations
HC regulations
Source data
Regulatory binders
IRB submissions
Subject visits
Lab work
Investigational product

Nice to have

Medidata Rave
INFORM
Veeva Vault

Role summary

ClinSurge Research is seeking a Clinical Research Assistant - Lab Technician for an on-site role. This position supports clinical trials by assisting with patient recruitment, data collection and entry into EDC systems, maintaining regulatory binders, and coordinating study-related activities like phlebotomy and lab work. The role requires a Bachelor's degree in life sciences or a related field, 0-2 years of experience in clinical research or healthcare, and phlebotomy certification. Familiarity with GCP, ICH, FDA, and HC regulations is a plus, as is experience with EDC systems. Exceptional organizational skills and attention to detail are essential.

Clinical Research Assistant - Lab Technician (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 - Lab Technician 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, phlebotomy, 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)
Phlebotomy certification and with experience and proficiency
Familiarity with GCP, ICH guidelines, and FDA & HC regulations is a strong 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

Ready to apply?

You'll be redirected to ClinSurge Research's application page.