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Clinical Research Coordinator I

4 months ago

Toronto, Canada University Health Network Full time

**JOB TITLE: Clinical Research Coordinator I**

**Job Posting #: 923698**

**Union**:Non-Union

**Site**: Princess Margaret Research Institute

**Department**: Surgical Oncology - Breast

**Reports to**: Clinical Research Manager

**Hours**: 37.5 work hours per week

**Salary range**:$66,565 - $83, 207 per annum**:To **commensurate** with experience and consistent with UHN compensation policy**

**Status**: Temporary Full Time (1 year, with possibility of extension)

**Pos**ted** Da**te**: August 24, 2023

**Closing Date**: September 30, 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.

**Job Summary**:
The Department of Surgical Oncology requires a Clinical Research Coordinator I to work with various research projects and initiatives under its Reconstructive Breast Cancer surgery portfolio. Working under the guidance of the Principal Investigators and the Clinical Research Manager, the Clinical Research Coordinator I collaborates with the Investigators to jointly assume responsibility for the overall management and coordination of surgical clinical research studies and academic activities.

This role requires previous experience in the coordination and administration of clinical studies (patient contact and informed consent; implements and coordinates all aspects of data collection and source documentation, as per UHN policy and ICH/GCP guidelines; identification of problems using assessment skills; and of execution study-related administrative tasks, such as collection of regulatory documents, research ethics board submissions, assessment of study-related literature). The role also requires solid experience in statistical analysis, including multivariate analyses.

**Duties**

In addition to clinical research project activities, responsibilities include but are not limited to;
- Protocol development, manuscript and abstract preparation, conference preparation, statistical analysis, data collection and cleaning, and grant funding submission & management.
- The Clinical Research Coordinator I will also work with medical trainees to provide support and guidance throughout various research projects and initiatives.

The CRC I role is a primarily on-site position, with some flexibility for work from home as clinical schedule and tasks allow and as approved by the Manager and PIs in accordance with UHN guidelines.

**Qualifications**:

- Bachelors degree, or recognized equivalent, in a health or science-related discipline
- Minimum three (3) years of clinical and/or professional experience, minimum of 1 year clinical research experience
- Certification as a Clinical Research Professional (e.g. SOCRA, ACRP), preferred
- Experienced with statistical software and ability to conduct statistical analysis independently, required
- Proficiency in basic medical, and surgical terminology required
- Background or understanding of human anatomy, asset
- Previous research in oncology, strongly preferred
- Experience with patient contact including informed consent and quality of life questionnaire administration
- Demonstrate relevant clinical research funding/budgeting knowledge
- Experience with grant writing, management, and reporting
- Experience with manuscript preparation and scientific writing
- Experience with protocol and study document development
- Demonstrated ability to train other team members, asset
- Experience with research ethics submissions and maintenance
- Knowledge of ICH/GCP guidelines
- Excellent organizational and time management skills required
- Excellent interpersonal, verbal and written communication skills
- Ability to set priorities and work independently with accuracy in a multitasking environment
- Able to operate effectively in an interdisciplinary team
- Strong Proficiency with MS Office software, Word, Excel, Outlook

**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, now and through