Clinical Research Assistant - Lab Technician at ClinSurge Research — NeverHard
Clinical Research Assistant - Lab Technician at ClinSurge Research in Mississauga, Peel region. Skills: Attention to Detail, Data Entry, GCP, Phlebotomy, Regulatory Compliance. Apply on NeverHard.
Company
ClinSurge Research
Location
Mississauga, Peel region
Type
not_specified
Required skills:
Attention to Detail
Data Entry
GCP
Phlebotomy
Regulatory Compliance
Job DescriptionJob DescriptionClinical 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
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