Clinical Research Assistant - Lab Technician
- Mississauga, ON, L5K 2L3, 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
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 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
The role involves assisting with patient recruitment, screening, and enrollment while maintaining accurate data in electronic capture systems. You will also coordinate subject visits, perform phlebotomy, and manage regulatory documentation in compliance with GCP guidelines.
Requirements
Candidates must hold a bachelor's degree in life sciences or a related field and possess phlebotomy certification. Proficiency in clinical research protocols and familiarity with FDA and ICH regulations are highly desired.
Skills
- Clinical research
- Phlebotomy
- Data entry
- GCP compliance
- Patient recruitment
- Regulatory documentation
- EDC systems
- Medidata Rave
- INFORM
- Veeva Vault
- Protocol management
- Investigational product accountability
- Attention to detail
- Communication skills
- Organizational skills
Visa sponsorship
Not detected in the job text
Categories
- Science & Research
- Healthcare
- Administrative
Keywords
- Clinical Research Assistant
- Lab Technician
- Clinical Trials
- GCP
- ICH Guidelines
- FDA
- HC Regulations
- EDC
- Medidata Rave
- INFORM
- Veeva Vault
- Phlebotomy
- IRB
- Patient Recruitment
- Source Data Verification
- Regulatory Binders
- Investigational Product
- Life Sciences
- Public Health
- Clinical Research Organization