Posted 17 days ago
Clinical Research Assistant - Lab Technician
@ ClinSurge Research
Mississauga, Ontario
Overview
ClinSurge Research is hiring a Clinical Research Assistant - Lab Technician for a full-time, on-site role supporting its clinical trial portfolio. The work covers patient recruitment and screening, source data handling, EDC data entry, regulatory binders, subject visits with phlebotomy, and monitoring-visit preparation.
Responsibilities:
- Recruit, screen and enroll patients across active protocols
- Collect, verify and enter source data per GCP and EDC systems
- Schedule subject visits, phlebotomy and investigational product dispensing
- Maintain regulatory binders and IRB submissions
- Prepare for sponsor monitoring visits and audits
Requirements summary:
- Bachelor's degree in life sciences, public health or related field
- 0-2 years clinical research or healthcare experience
- Phlebotomy certification and proficiency
- Familiarity with GCP, ICH, FDA and Health Canada regulations (asset)
- Experience with EDC systems such as Medidata Rave or Veeva Vault (asset)
Tools & skills
Source and dates
Employer career site / ATS feed · jazzhr
- Employer posting date
- 2026-10-21
- First seen by our source
- 2026-10-22
- Source record updated
- 2026-10-22
These dates describe the source record, not a live verification that the employer is still hiring. Check the original posting.
Job details
| Seniority | Entry level |
| Department | Allied health |
| Experience | 0+ years |
| Hours per week | 40 (estimated) |
| Travel | air: none · ground: none |
| Work setting | Office, Client sites |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Languages | English |
| Licences & certifications | Phlebotomy certification |
| Education | Bachelor’s degree (required) |
| Fields of study | life sciences, public health |
Summary and details written by AI from the posting; the employer’s posting is the authority.
ClinSurge Research
Saved company profile
Historical company information from a saved The Jobs API profile (LinkedIn/Crunchbase fields). It is not live-verified; figures may have changed. Missing values remain unknown.
Full company description
At ClinSurge Research, we are dedicated to transforming healthcare through innovative clinical research.
- LinkedIn followers
- 2,565
- People associated on LinkedIn
- 18
- Other recorded names
- ClinSurge Research
- Profile identifies a recruitment agency
- No
At ClinSurge Research, we are dedicated to transforming healthcare through innovative clinical research.
| Field | Value |
|---|---|
| Industry | Research Services |
| Company size | 11-50 employees |
| Organization type | Privately Held |
| Year founded | 2025 |
| Open jobs on Jobsy | 5 |
| View page |
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
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