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Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-159[...]
Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-159[...]Sunnybrook • Toronto, ON, CA
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Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-159[...]

Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-159[...]

Sunnybrook • Toronto, ON, CA
Il y a 16 jours
Type de contrat
  • Temps plein
Description de poste

Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences

Join to apply for the Clinical Research Coordinator (SRI) - Evaluative Clinical Sciences - Regular Full-time 2025-15904 role at Sunnybrook .

Major Responsibilities

  • Identifying and recruiting potential research study participants via phone or in person by conducting interviews and obtaining patient consent
  • Reviewing patient charts to determine eligibility
  • Arranging and booking follow-up appointments by communicating and liaising effectively with other Hospital groups
  • Answering study participants’ questions and navigating them throughout the study by effective communications
  • Collecting, updating and managing study and participants’ data, completing CRFs, performing data entry and preparing special reports as required by the study investigators.
  • Assist with amendments to study documents, ICFs and SOPs for Research Ethics submissions as well as regulatory file maintenance.

Additional Responsibilities

  • Work within the larger context of SHSC and observe the Hospital’s and Research Institute’s rules and regulations, policies, procedures, practices, safety procedures and current legislation, in particular the Good Clinical Practices standards. Ensure the confidentiality of patient, employee, graduate student and Hospital information at all times.
  • Work cooperatively and constructively with the other members of SHSC staff.
  • Perform the above functions in a manner which reflects the Hospital’s philosophy and mission of service, while promoting and maintaining good public relations with patients, visitors and Hospital staff.
  • Understand the requirements of the various controlling bodies, agencies and frameworks, guiding the project and conforming to those requirements including any necessary audit processes.

    • Education, Skills and Experience

  • At minimum, completion of bachelor’s degree in health sciences, or equivalent, required.
  • At least two (2) years of clinical / trial coordination experience and / or one (1) year of research experience or training is preferred
  • Excellent patient interviewing and evaluation skills
  • Demonstrated effective communication, critical thinking, and interpersonal skills
  • Knowledge of medical terminology in the areas of gynecology and urology is preferred.
  • Previous word-processing, database and spreadsheet software experience, in a Microsoft Office environment, including Excel, Word, PowerPoint and Electronic Patient Record Databases
  • Knowledge of ICH / GCP regulations and guidelines
  • Excellent organizational and time management skills with an attention to detail
  • Excellent interpersonal and client service skills
  • Excellent presentation and facilitation skills
  • Self motivated and able to work independently as well as within a team
  • Ability to produce high quality work in accordance with Hospital standards
  • Ability to work well under pressure and use of good judgment in assessing and responding to difficult situations
  • Ability to maintain confidentiality and strong knowledge of clinical ethics regulations
  • Comprehensive knowledge of hospital organizational / office practices, procedures and standards
  • Experience working in a health care, scientific or research environment preferred.
  • Must be flexible to work Monday to Friday within the times of from 8 : 00 am to 4 : 00 pm

    • Qualified applicants are invited to submit a resume.

    We thank all applicants for their interest; however, only candidates selected for an interview will be contacted.

    Sunnybrook Health Sciences Centre 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 Health Sciences Centre 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, LGBTQ persons, and all others who may contribute to the further diversification of ideas.

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