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Senior Research Coordinator

Baycrest
Toronto, Ontario, Canada
$97.5K a year (estimated)
Temporary

Responsibilities include but are not limited to : Responsibilities include but are not limited to :

  • Acts as a Leader by advising Research Assistants, Trainees, Phlebotomists, and Safety Staff on proper trial execution based on protocol, Standard Operating Procedures (SOPs), and regulatory requirements.
  • Conducts clinical in-person assessments with study participants (including height, weight, blood pressure, physical activity, sensorimotor functioning, DEXA, ultrasound, cognition, etc.)
  • Conducts vital signs collection and assessment
  • Monitors, records, and report symptoms and changes in study participants conditions
  • Completes adverse event and serious adverse event reports and file with regulatory bodies
  • Contributes to Research Ethics Board (REB) submissions and communications, including year-end and donor reports
  • Responds to and / or assists with on-site emergencies, incidents and accidents, which may involve the provision of Standard First Aid, CPR, the use of an Automated External Defibrillator (AED) and / or the completion of an accident / incident report, when required
  • Demonstrates ability to effectively communicate with clients and families
  • Qualifications include but are not limited to :
  • Completed postsecondary degree in a science or healthcare related discipline, or equivalent work experience.
  • Certification as a Clinical Research Professional (SOCRA, ACRP, etc.)
  • Current GCP, Health Canada Part C Division 5, IATA certifications
  • Phlebotomy certification
  • Certification in genetic counselling strongly preferred
  • 2-3 years previous research or clinical trials experience preferred and / or a definite asset, particularly with older adult clientele and 3-5 years’ work experience as a Clinical Research Coordinator
  • Extensive knowledge about cognitive, brain, and physical aging and the common tools and measures to assess them
  • Current GCP and familiarity with Health Canada, FDA, ICH GCP regulations
  • Excellent computer skills and ability to adapt to new technologies.
  • Knowledge of Freedom of Information and Protection of Privacy Act 1990 (FIPPA) requirements, as well as the Personal Health Information Protection Act 2004.
  • Excellent verbal, written, and listening skills.
  • Ability to document concisely and appropriately.
  • Good client-focused service approach.
  • Demonstrated ability to effectively communicate with clients and families.
  • Ability to work effectively with a range of stakeholders
  • 30+ days ago
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