Clinical Research Assistant - Lab Technician
- Mississauga, ON, Canada
Full-time
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Job details
- Job type
- Full-time
- Apply by
- Experience
- 0–2 years of experience in a clinical research or healthcare setting (internships welcome)
- Posting language
- English
- Posted
Original job description
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 overviewWe 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
- 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
More about this job
Responsibilities
Support clinical trials by assisting with patient recruitment, screening, enrollment, visit scheduling, phlebotomy, and laboratory work. Maintain accurate study data and regulatory documentation, coordinate with sponsors, CROs, and IRBs, and help prepare for monitoring visits and audits.
Requirements
A bachelor's degree in life sciences, public health, or a related field is required, along with 0–2 years of clinical research or healthcare experience; internships are welcome. Phlebotomy certification and experience are requested, while familiarity with GCP, ICH guidelines, FDA and Health Canada regulations, and EDC systems is an advantage.
Skills
- Patient Recruitment
- Patient Screening
- Patient Enrollment
- Clinical Trial Coordination
- Source Data Collection
- Good Clinical Practice (GCP) Compliance
- Electronic Data Capture (EDC)
- Regulatory Documentation
- Subject Visit Scheduling
- Phlebotomy
- Laboratory Coordination
- Investigational Product Accountability
- Sponsor and CRO Communication
- Regulatory Audit Preparation
- Organization
- Written and Verbal Communication
Visa sponsorship
Not detected in the job text
Categories
- Healthcare
- Science & Research
- Administrative
Keywords
- Clinical Research
- Clinical Trials
- Patient Recruitment
- Patient Screening
- Patient Enrollment
- Good Clinical Practice (GCP)
- ICH Guidelines
- FDA Regulations
- Health Canada Regulations
- Electronic Data Capture (EDC)
- Medidata Rave
- INFORM
- Veeva Vault
- Phlebotomy
- Source Data
- Study Protocols
- Regulatory Binders
- IRB Submissions
- Essential Documents
- Sponsor Monitoring
- Regulatory Audits
- Investigational Product Accountability
- Principal Investigators
- Study Coordinators
- CROs