Clinical Research Coordinator 2 (SRI)-Regular Full-time 2025-14468 (2025-14468)

Sunnybrook


Date: 3 days ago
City: Toronto, ON
Contract type: Full time
Summary Of Duties

  • Function as part of a interdisciplinary, patient-focused team of professionals to ensure smooth and efficient facilitation of clinical trial activities
  • Lead the day-to-day activities of a clinical trial including pre-screening/screening and recruiting eligible participants, obtaining informed consent, collecting and managing study data and ensuring compliance with protocols and regulatory guidelines
  • Initiate, manage, and coordinate submissions to Research Ethics Board and contracts for Legal Review
  • Communicate with internal hospital departments to complete impact assessments, facilitate departmental research agreements and obtain institutional approvals
  • Financial duties relating to clinical trial activities including budget development, invoicing and study-related patient reimbursements
  • Establish, maintain and complete all essential documents in Investigator Site File (ISF) ensuring adherence to regulatory requirements
  • Coordinate patient follow-up visit schedules as per study protocol and execution of all aspects of study visits including protocol specific assessments such as obtaining patient vitals, electrocardiograms and sample collection/processing
  • Report Adverse Events/Serious Adverse Events as per protocol and sponsor requirements
  • Liaise with sponsors as required
  • Prepare for monitoring visits, audits and inspections
  • Support the development and execution of high level strategic initiatives within the Nephrology research program

Qualifications

  • Minimum 5 years of clinical research experience in a hospital setting
  • Bachelor’s degree in health-related field required, Master’s degree is an asset
  • Recognized certification in clinical research (ACRP or SOCRA) is an asset
  • Training and experience or willingness to be trained in Phlebotomy/Venipuncture practice required
  • Demonstrated knowledge of research regulations and guidelines (ICH/GCP, Health Canada, Tri-Council Policy, Declaration of Helsinki, etc.)
  • Advanced proficiency in computer skills (Microsoft Office: Word, Excel, PowerPoint, Adobe)
  • Experience with Clinical Trial Management Systems and Electronic Data Capture systems an asset
  • Strong oral and written communication skills
  • A “can do” attitude: Flexibility to work in a complex environment with ability to multitask and prioritize to meet deadlines
  • Demonstrates initiative and the ability to work effectively both independently to take lead on assigned projects and as part of a team

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