Clinical Research Coordinator (North York)

Clinical Research Coordinator (North York)

17 Sep
|
North York Diagnostic u0026 Cardiac Centre
|
North York

17 Sep

North York Diagnostic u0026 Cardiac Centre

North York

Overview:

North York Diagnostic & Cardiac Centre (NYDCC) is seeking an experienced and highly organized Clinical Research Coordinator (CRC) to join our growing clinical research team.

The CRC will be responsible for the day-to-day coordination and execution of clinical trials at the site level, working closely with Principal Investigators, Sub-Investigators, sponsors, CROs, monitors, research staff, and study participants.

This is a hands-on position suited to someone who is comfortable managing multiple clinical trials and participant visits in a fast-paced research environment while maintaining a strong focus on participant safety, protocol compliance, data quality, and regulatory requirements.

Key Responsibilities:

- Coordinate and manage assigned clinical trials from study start-up through close-out
- Identify, pre-screen, recruit, screen, and enroll potential study participants
- Coordinate and conduct study visits in accordance with approved protocols and visit schedules
- Obtain and document informed consent in accordance with applicable regulations, GCP, and site procedures
- Complete source documentation and enter study data into electronic data capture (EDC) systems accurately and within required timelines
- Maintain complete and audit-ready study documentation and regulatory files
- Coordinate laboratory testing, diagnostic procedures, investigational product requirements, and other protocol-specific activities
- Perform phlebotomy and process biological samples when required and appropriately trained
- Identify, document, and escalate adverse events, serious adverse events, protocol deviations, and other safety-related information
- Maintain study trackers, participant logs, delegation logs, training documentation, and other essential study records
- Prepare for and participate in Site Initiation Visits, Monitoring Visits, audits, and study close-out activities
- Address monitoring follow-up items and work collaboratively with the research team to resolve outstanding study requirements




- Communicate regularly with investigators, sponsors, CROs, monitors, and other study stakeholders
- Ensure all study activities are conducted in accordance with the protocol, ICH-GCP, Health Canada requirements, applicable regulations, and site SOPs
- Support other members of the research team as required to ensure efficient and compliant study operations

Qualifications:

- Previous experience as a Clinical Research Coordinator or in a similar clinical research role is strongly preferred
- Experience with Phase II and/or Phase III clinical trials is an asset
- Strong understanding of clinical trial processes, informed consent, source documentation, and regulatory requirements
- Knowledge of ICH-GCP and Health Canada clinical research requirements
- Experience working with EDC, IRT/IWRS, electronic study portals, and other clinical trial systems is an asset
- Strong knowledge of medical terminology
- Phlebotomy experience is an asset
- Cardiovascular clinical research experience is an asset but not required
- Excellent organizational and time-management skills
- Robust attention to detail and commitment to accurate, contemporaneous documentation
- Ability to manage multiple studies, priorities, and deadlines simultaneously
- Strong written and verbal communication skills
- Ability to work both independently and collaboratively within a multidisciplinary research team
- Medical, nursing, life sciences, or other healthcare-related education is preferred

What We Offer:

NYDCC offers the opportunity to work within an active and growing clinical research program alongside experienced investigators and research professionals. Our team conducts a diverse portfolio of clinical trials and provides opportunities to develop experience across multiple studies, sponsors, and therapeutic areas.

We are looking for someone who is organized, accountable, collaborative, detail-oriented, and committed to maintaining high standards in clinical research.

Pay: $22.00-$33.00 per hour

Benefits

- On-site parking

Work Location: In person

📌 Clinical Research Coordinator (North York)
🏢 North York Diagnostic u0026 Cardiac Centre
📍 North York

Reply to this offer

Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.

Subscribe to this job alert:

Get the latest job offers by email for: clinical research coordinator (north york) / north york

Subscribe to this job alert:

Get the latest job offers by email for: clinical research coordinator (north york) / north york