Clinical Research Coordinator I

3 weeks ago

Toronto, Canada University Health Network Full time

**JOB TITLE: Clinical Research Coordinator I**

**Job Posting #: 922728**

**Site**:Princess Margaret Cancer Centre

**Department**:Joint Department of Medical Imaging (JDMI)

**Reports to**:Research Manager and Investigators

**Hours**:37.5 hrs Per Week

**Salary: $66,565.00 - $83,206.50** annually. To commensurate with experience and consistent with UHN compensation policy

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

**Posted Date: July 21, 2023**

**Closing Date: Until filled**

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**

**University Health Network (UHN)** is looking for an experienced professional to fill the key role of **Clinical Research Coordinator I** in our **JDMI** Department.

The Joint Department of Medical Imaging requires a Clinical Research Coordinator I to work with its clinical research portfolio in accordance with ICH/GCP guidelines, Tri-Council policies, applicable regulations, and hospital and departmental guidelines under the direction of the Research Program Manager and Principle Investigators.

**Duties**

The Clinical Research Coordinator requires previous experience in the coordination and administration of clinical studies. Primary responsibilities will include, but are not limited to;
- Coordinating patient visits and schedule as per study protocol; executing all aspects of study visit (e.g., documentation of adverse events & treatment administration management;
- Coordination of required tests/procedures/sample collection) according to approved protocol; planning, reviewing and coordinating all aspects of data collection and source documentation as per UHN policy and ICH/GCP guidelines;
- Reporting any study related abnormalities as per defined parameters; renewing and amending research ethics approval or HC CTA as needed;
- Monitoring and promoting the quality and integrity of data, recording clinical trial data in case report forms (CRF’s), and compilation of ethics and regulatory documents; liaising with sponsors for monitoring/audits; facilitating hosting of regulatory inspections.
- In addition to clinical research activities, the Clinical Research Coordinator I will also be an active contributor in helping with literature search, editing and submission of research manuscripts and taking part in design and evaluation of study protocols.

**Qualifications**
- Bachelor’s degree in a health or science-related discipline or equivalent
- Recognized certification in clinical research (ACRP or SOCRA) preferred
- Minimum three (3) years appropriate clinical and/or professional experience
- Minimum one (1) year oncology and/cardio-vascular clinical research experience preferred
- Demonstrated knowledge of applicable research regulations and guidelines such as ICH/GCP and Tri-Council Policy
- Previous experience with oncology and or/cardio-vascular clinical trials and/or PI initiated trials is preferred
- Knowledge of Medical Imaging is an asset
- Venipuncture certification /experience preferred
- Knowledge of IATA shipping regulations and basic laboratory procedures an asset
- Demonstrated attention to detail
- Exceptional organizational & time management skills
- Ability to multi-task & perform in a fast-paced environment
- Well developed leadership skills; self-motivated
- Ability to work well independently as wall as part of a team
- Strong analytical & problem-solving skills
- Mentor/training experience is an asset
- Strong verbal and written communication skills
- Excellent listening, conflict resolution skills
- Proficiency with Microsoft Office Software (Outlook, Word, Excel, PowerPoint)
- 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.

**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

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