Clinical Research Analyst

University Health Network • Toronto, ON

10d • CA$65,919 - CA$82,389 • Onsite

About The Position

We are looking for a highly motivated individual with prior clinical and translational research experience to join our research team at the Department of Medical Oncology and Hematology. Working under the direction of the program lead, clinical research manager, and Principal Investigators, the successful candidate will be responsible for the oversight, organization and coordination of investigator-led and sponsored studies.

Requirements

• Bachelors Degree in a health or science-related field or equivalent
• Minimum 2 years clinical research experience and experience with patient contact
• Knowledge of research regulations and guidelines, such as ICH/GCP guidelines, Tri-Council Policy, Declaration of Helsinki and FDA CFR and Health Canada TPD
• Ability to perform duties in a professional and courteous manner and produce high quality work while meeting deadlines in accordance to UHN standards
• Strong verbal & written communication skills
• Exceptional organizational & time management skills & attention to detail
• Ability to multi-task & perform with accuracy in a fast-paced environment
• Well-developed leadership & excellent interpersonal skills
• Self-motivated; ability to work well independently as well as part of a team
• Strong analytical & problem solving skills
• Excellent decision-making, listening & conflict resolution skills

Responsibilities

• Specific tasks will include daily administrative research operations, interfacing and coordinating with patients and a team of scientists and knowledge users, preparing, and maintaining REB applications, research proposals and maintaining meticulous study records in compliance with study protocols.
• Recruit study participants (e.g. identify, screen potential participants & obtain informed consent)
• Day-to-day coordination of research biospecimen collections
• Maintain file documentation, such as collection of regulatory documents, submission to the Research Ethics Board and other regulatory agencies as required
• Prepare study documents and templates (i.e. CRFs, study logs) and coordinate all aspects of data collection and source documentation as per UHN policy and ICH/GCP guidelines
• Manage REDCap Database - abstract, review and monitor clinical data in research databases

Benefits

• Competitive offer packages
• Government organization and a member of the Healthcare of Ontario Pension Plan (HOOPP)
• Close access to Transit and UHN shuttle service
• A flexible work environment
• Opportunities for development and promotions within a large organization
• Additional perks (multiple corporate discounts including: travel, restaurants, parking, phone plans, auto insurance discounts, on-site gyms, etc.)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level