Posted 2 months ago
Clinical Research Coordinator
@ ClinSurge Research
Nepean, Ontario
Overview
ClinSurge Research is hiring a full-time Clinical Research Coordinator to manage and coordinate clinical research studies under Good Clinical Practice, institutional guidelines and federal regulations. The role covers participant recruitment, consent, data collection, regulatory documentation and adverse event reporting, on-site in a physician practice and clinical research setting. The posting requires a bachelor's degree in a health or life science field and states that phlebotomy certification is required, with preferred experience of 1-3 years.
Responsibilities:
- Coordinate and conduct clinical research studies, including recruitment, consent and follow-up
- Ensure compliance with protocols and Health Canada, IRB and ICH-GCP requirements
- Collect and enter data into EDC systems
- Maintain regulatory binders, subject files and case report forms
- Monitor and report adverse events and prepare for monitoring visits and audits
Requirements summary:
- Bachelor's degree in health sciences, life sciences, nursing or related field (required)
- 1-3 years clinical research experience (preferred)
- CCRC or CCRP certification (asset)
- Phlebotomy certification and IATA shipping knowledge
- Strong knowledge of GCP, Health Canada and IRB regulations
- Proficiency with EDC systems and Microsoft Office
Tools & skills
Source and dates
Employer career site / ATS feed · jazzhr
- Employer posting date
- 2026-09-13
- First seen by our source
- 2026-10-09
- Source record updated
- 2026-10-16
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 |
| Hours per week | 40 (estimated) |
| Travel | air: none · ground: none |
| Work setting | Hospital or clinic, Laboratory, Office |
| Position | Sitting and standing |
| Physical demands | physical low · computer high |
| Licences & certifications | Phlebotomy certification, CCRC, CCRP |
| Education | Bachelor’s degree (required) |
| Fields of study | health sciences, life sciences, nursing |
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 |
Position Summary:
We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to manage and coordinate clinical research studies in accordance with Good Clinical Practice (GCP), institutional guidelines, and federal regulations. The CRC will work closely with investigators, sponsors, and participants to ensure the integrity of study protocols and data collection.
Key Responsibilities:
- Coordinate and conduct all aspects of clinical research studies, including participant recruitment, consent, scheduling, and follow-up.
- Ensure compliance with study protocols and regulatory requirements (Health Canada, IRB, ICH-GCP).
- Collect and enter data accurately into electronic data capture (EDC) systems.
- Maintain study documents, including electronic regulatory binders, subject files, and case report forms.
- Monitor and report adverse events and ensure timely communication with the IRB and sponsors.
- Prepare for and participate in monitoring visits, audits, and inspections.
- Collaborate with cross-functional teams, including principal investigators, sponsors, and other research personnel.
Qualifications:
- Bachelor’s degree in health sciences, life sciences, nursing, or a related field (required).
- Minimum [1-3] years of experience in clinical research (preferred).
- Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Professional (CCRP) a plus.
- Phlebotomy certification and proficiency in drawing with ability to process and ship per IATA requirements.
- Strong knowledge of GCP, Health Canada, and IRB regulations.
- Excellent organizational, communication, and problem-solving skills.
- Proficiency with EDC systems (e.g., Medidata, or RAVE) and Microsoft Office Suite.
Work Environment:
- On-site in physician practice and clinical research setting.
- May require handling of biological samples and/or working with patients.
Journal
Only you can see this. Kept on this device, and in your account when you sign in.