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Clinical Research Coordinator at ClinSurge Research

Ottawa, Ontario, Canada -

Full Time

Start Date

Immediate

Expiry Date

16 Oct, 26

Salary

0.0

Posted On

18 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research Coordination, Participant Recruitment, GCP Compliance, Data Collection, EDC Systems, Regulatory Documentation, Adverse Event Reporting, Phlebotomy, IATA Shipping, Problem-solving, Communication, Organization

Industry

Research Services

Description

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.

Responsibilities

The coordinator manages clinical research studies by handling participant recruitment, consent, and data entry into EDC systems. They ensure strict compliance with GCP, Health Canada, and IRB regulations while collaborating with investigators and sponsors.