Clinical Research Coordinator
at
ClinSurge Research
Ontario, Ontario, Canada
-
Full Time
Start Date
Immediate
Expiry Date
23 Nov, 26
Salary
0.0
Posted On
25 Aug, 26
Experience
0 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
Yes
Skills
Industry
Hospitals & Health Systems
Description
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.
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