Clinical Research Analyst - Toronto, Canada - University Health Network

University Health Network
University Health Network
Verified Company
Toronto, Canada

4 weeks ago

Sophia Lee

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Sophia Lee

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Full time
Description
**Job Title: Clinical Research Analyst


Job Posting #: 925965

Union:
NON-UNION


Site:
Princess Margaret Cancer Center


Department:
Division of Medical Oncology and Hematology, Multiple Myeloma and Related Diseases

  • Clinical Trials

Diseases:
Clinical Trials


Reports to:
Clinical Research Manager


Hours:37.5 hrs. per week


Salary:
$
62,135 minimum: To **Commensurate with experience and consistent with the UHN Compensation Policy)

Status:
Temporary Full-Time (Hybrid, after probation period), with the opportunity to extend to a Permanent Full Time position


Posted Date:
November 1, 2023

Closing Date:
November 15, 2023


The University Health Network, where "above all else the needs of patients come first", encompasses Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute and the Michener Institute of Education.

The breadth of research, the complexity of the cases treated, and the magnitude of its educational enterprise has made UHN a national and international resource for patient care, research and education.

With a long tradition of ground breaking firsts and a purpose of "Transforming lives and communities through excellence in care, discovery and learning", the University Health Network (UHN), Canada's largest research teaching hospital, brings together over 16,000 employees, more than 1,200 physicians, 8,000+ students, and many volunteers.

UHN is a caring, creative place where amazing people are amazing the world.


Position Summary


The Division of Medical Oncology and Hematology, University Health Network requires a Clinical Research Analyst (CRA) to work with its clinical trial portfolio for Multiple Myeloma and Related Diseases.

The CRA participates in the implementation and coordination of clinical trials from protocol (Investigator Initiated or Industry Sponsored) review and approval through to activation, follow up and trial closure.


Duties:


Principal responsibilities include:

  • Monitoring and promoting the quality and integrity of data, recording clinical trial data in case report forms (CRF's) or Electronic Data Capture (EDC), and compilation, submission and maintenance of ethics and regulatory documents.
  • The coordination and monitoring of data is performed in accordance with the trial protocol, hospital and departmental guidelines and professional standards of practice. Data is assessed, compiled, recorded and submitted to cooperative groups and/or pharmaceutical companies or used for internal Princess Margaret Cancer Centre investigator initiated studies.
  • All data must be complete, accurate, timely and must be in compliance with applicable ICH-GCP, FDA and US federal code and Tri-Council regulations.
  • The CRA must be able to interpret the data gathered from source and the applicable regulations in order to ensure compliance. Quality assurance procedures are utilized to ensure high quality data is obtained.
  • Additionally, the CRA liaises between site and sponsor to ensure that all trialrelated documentation and information are distributed to relevant staff and designs and implements quality assurance tools to enhance data quality and optimize adherence to protocol.

Qualifications:


  • At minimum, a completion of a Bachelor's degree program, or recognized equivalent in Health or Science Related Discipline
  • At least one (1) to two (2) years of experience in Oncology (preferred) and/or Clinical trials.
  • Demonstrated relevant clinical research and medical terminology knowledge, familiarity with Health Canada CTA submissions, previous experience in oncohematological disease sites is an asset
  • Excellent written and verbal communication skills, excellent organization, prioritization skills, good computer skills, ability to learn quickly and work independently
  • Excellent interpersonal skills
  • Ability to work under pressure with attention to detail
  • Ability to perform duties in a professional and courteous manner and produce high quality work while meeting deadlines in accordance to UHN standards
  • Ability to perform multiple concurrent tasks
  • Knowledge of applicable legislative, UHN and/or departmental policies
  • Client service oriented, with the ability to effectively work with diversity and appreciate that people with different opinions, backgrounds and characteristics bring richness to the challenge or situation at hand
  • Satisfactory attendance
  • Certification as a Clinical Research Professional (SoCRA) preferred, or working towards obtaining it.
  • Proficiency with MS Office, Excel, Power Point, or equivalent software required.

Why join UHN?


In addition to working alongside some of the most talented and inspiring healthcare professionals in the world, UHN offers a wide range of benefits, programs and perks.

It is the comprehensiveness of these offerings that makes it a differentiating factor, allowing you to find value where it matters most to you,
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