Clinical Research Coordinator: Drive Study Operations

Search Influence

Hamilton

On-site

CAD 55,000 - 75,000

Full time

5 days ago

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Job summary

Search Influence is seeking a motivated Clinical Research Coordinator to manage studies in a physician practice and clinical research setting. You will coordinate participant recruitment, consent, data entry in EDC, and regulatory compliance under GCP, Health Canada and IRB guidelines.

The role requires a Bachelor’s in health sciences or related field, 1–3 years of clinical research experience, and proficiency with Medidata/RAVE and MS Office; phlebotomy certification is a plus.

Qualifications

Bachelors degree required.
13 years clinical research experience preferred.
CCRC or CCRP certification a plus.
Phlebotomy certification and proficiency in drawing per IATA requirements.
Strong knowledge of GCP, Health Canada, and IRB regulations.
Proficiency with EDC systems (Medidata, RAVE) and MS Office.
Excellent organizational and communication skills.

Responsibilities

Coordinate all aspects of clinical studies, including recruitment, consent, scheduling, and follow-up.
Ensure compliance with study protocols and regulatory requirements.
Collect and enter data into EDC systems.
Maintain study documents, including electronic regulatory binders, subject files, and case report forms.
Monitor and report adverse events and communicate with IRB and sponsors.
Prepare for monitoring visits, audits, and inspections.
Collaborate with investigators, sponsors, and other research personnel.