Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-131[...]

Sunnybrook; Toronto; On-site; CAD 60,000 - 90,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to lead and manage clinical studies in a dynamic healthcare environment. This role involves collaborating with healthcare teams and external sponsors while ensuring compliance with regulatory guidelines. You will be responsible for patient recruitment, data management, and protocol adherence, making a significant impact on advancing clinical research. If you are passionate about healthcare and have a strong background in research, this is an exciting opportunity to contribute to groundbreaking studies and improve patient outcomes.

Qualifications

• Minimum 3 years of experience in recruiting human subjects for clinical studies.
• Certification as Clinical Research Professional (CCRP) or Coordinator (CCRC) is an asset.

Responsibilities

• Coordinate patient recruitment and manage study data.
• Ensure protocol requirements are accurately implemented by all staff.

Skills

Research Ethics Understanding

Data Collection and Management

Excellent Communication Skills

Organizational Skills

Interpersonal Skills

Education

Bachelor’s Degree in Health Sciences

Tools

Word Processing Software

Advanced Database Management

Job description

Sunnybrook Health Sciences Centre is a leader in transcatheter aortic valve implantation (TAVI) for severe aortic stenosis, Interventional Cardiology, advanced cardiac imaging and cardiac electrophysiology in Canada, and is participating in a number of international and national clinical trials and registries in these areas.

The Clinical Research Coordinator will collaborate with investigators, health care teams and external sponsors to assume the responsibility for the overall management and coordination of these clinical studies according to regulatory and institutional guidelines and requirements.

Key Responsibilities/Tasks

• Perform specimen acquisition and handling.
• Perform review of electronic and paper charts including ECGs, vital signs, medical history, medications
• Collect and manage study data
• Coordinate patient recruitment through identifying and screening potential subjects, recruiting in- and out-patients and obtaining informed consent while working collaboratively with PI, clinical fellows, technical and nursing staff
• Ensure protocol requirements are implemented accurately by all staff and that subjects are following protocol requirements
• Coordinate patient follow up visit and schedules as per study protocol and execution of all aspects of study visits
• Coordinate general study management and administration
• Prepare informed consents and paperwork required by the Research Ethics Board
• Coordinate review and initiation of new studies
• Other duties related to the specific type of research assigned.
  
  

Qualifications

• Bachelor’s degree in a health sciences discipline
• Previous research experience (minimum 3 years) recruiting human subjects for clinical studies.
• A good understanding of research ethics (i.e. informed consent process, patient recruitment), ICH GCP, PHIPA, FDA and Health Canada regulations) and grant preparation an asset
• Experience in data collection, management and analysis
• Certification as a Clinical Research Professional (CCRP) or Clinical Research Coordinator (CCRC) is an asset
• Excellent Word Processing skills and Advanced Data Base skills an asset
• Excellent oral and written communication skills
• Outstanding skills in managing inter-personal interactions
• Strong organizational capabilities and ability to coordinate multiple projects, perform concurrent tasks, and work under pressure
• Demonstrated ability to work independently with initiative and accuracy.
  
  

Application screening will continue until a suitable candidate is identified. If your expertise qualifies you for this challenging position, please send a covering letter and resume.

We thank you in advance for your interest. Only those candidates selected for an interview will be contacted. No phone calls please.

Deadline for applications: Friday, May 30, 2025

Sunnybrook Research Institute is committed to providing accessible employment practices that are in compliance with the Accessibility for Ontarians with Disabilities Act (AODA). If you require accommodation for disability during any stage of the recruitment process, please indicate this in your cover letter.

Sunnybrook Research Institute is strongly committed to inclusion and diversity within its community and welcomes all applicants including but not limited to: visible minorities, all religions and ethnicities, persons with disabilities, 2SLGBTQ+ persons, and all others who may contribute to the further diversification of ideas.