17 May

Clinical Research Coordinator Jobs Vacancy in University Health Network Toronto

Position
Clinical Research Coordinator
Company
University Health Network
Location
Toronto ON
Opening
17 May, 2018 30+ days ago

University Health Network Toronto urgently required following position for Clinical Research Coordinator. Please read this job advertisement carefully before apply. There are some qualifications, experience and skills requirement that the employers require. Does your career history fit these requirements? Ensure you understand the role you are applying for and that it is suited to your skills and qualifications.

Follow the online directions, complete all the necessary fields, and provide all relevant information so your application is submitted correctly. When you click the 'Apply this Job' button (open in new window) you will be taken to the online application form. Here you will be asked to provide personal and contact details, respond to employment-related questions, and show how you meet the key selection criteria.

Clinical Research Coordinator Jobs Vacancy in University Health Network Toronto Jobs Details:

The Peter Munk Cardiac Center (PMCC) Cardiovascular Biobank is expanding, and we are looking to recruit a Clinical Research Coordinator I to help with accrual of patients into the PMCC CV Biobank. This position will require frequent interactions with patients, as well as with members of our team that includes physicians, nurses, trainees, as well as research staff. The position will create a bridge between the clinics/inpatients at PMCC and our research lab. Flexibility and adaptability, as well as outstanding communication skills are a must, as a rigor with documentation. Information on patient samples will need to be inventoried into a database and any experience with databases is an asset. Working knowledge of medical-legal policies and protocol for specimen handling and patient privacy are essential.

The CRC I will be responsible for accruing patients to translation research studies. This includes, but is not limited to, explaining the study protocol to the patients, answering questions, reviewing inclusion/exclusion criteria, and documenting the informed consent process. Other responsibilities include tracking biospecimens collected, creating study specific materials and workflows, attending regular team meetings, and keeping databases up to date.

Qualifications:
  • Bachelor's degree program, or recognized equivalent in a health or science related discipline.
  • 3 years clinical and/or professional experience
  • Up to 1 year clinical research experience, preferred
  • Excellent written and verbal communication skills
  • Exceptional interpersonal skills
  • History of direct communication with patients
  • Effective organizational, time management and prioritization skills
  • Ability to work independently and as a team member
  • Must be computer literate in Windows-based applications (eg. Word, Excel)

If you are interested in making your contribution at UHN, please apply on-line. You will be asked to copy and paste as well as attach your resume and covering letter. You will also be required to complete some initial screening questions.


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