Clinical Research Coordinator I

3 weeks ago

Toronto, Canada University Health Network Full time

**Position: Clinical Research Coordinator I**

**Job Posting #920887**

**Site**:Toronto Western Hospital

**Department**:Movement Disorders Clinic

**Reports to**: Clinical Research Manager and Principal Investigator

**Hours**: 37.5 hours per week

**Status**:Permanent Full Time

**Shifts**: N/A

**Posted Date**: June 08, 2023

**Closing Date**:July 08, 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**

Working under the direction of the Clinical Research Manager and Principal Investigator, the **Clinical Research Coordinator I (CRC I)** will collaborate with the study team to manage and coordinate multiple studies. This CRC I role is predominantly an on-site position.

**Duties**

Responsibilities of the position include, but may not be limited to:

- Recruitment of study participants (e.g. identifying, screening potential participants & obtaining informed consent)
- Coordinating complex patient visit schedules as per study protocol
- Planning, implementing, and coordinating all aspects of study visits including scheduling patient visits, arranging & uploading imaging scans, assisting with lumbar punctures & skin biopsies, documentation of adverse events & concomitant medications, administration of neuropsychological & cognitive questionnaires, sample collection, sample processing & shipping according to study protocol &, etc.
- Implementing and coordinating all aspects of data collection and source documentation as per UHN policy and ICH/GCP guidelines
- Executing study-related administrative tasks, such as collation of regulatory documents, submissions to the Research Ethics Board and other regulatory agencies as required, completion of relevant study CRFs, logs, and entering into databases in a timely manner & etc.
- Liaising with CROs/sponsors, external stakeholders & members of the clinical research team
- Preparing and liaising with CROs/sponsors for monitoring visits and/or audits
- Organizing and attending ongoing meetings
- Contributing to protocol development

**Qualifications**:

- Bachelor’s degree in a health or science-related field or equivalent
- Minimum 2 years of clinical research experience and experience with patient contact
- Prior experience in the coordination and administration of clinical trials
- Experience with research regulatory submissions is a strong asset
- Phlebotomy certification preferred
- TDG (Transportation of Dangerous Goods) certification preferred
- Knowledge of IATA (International Air Transport Association) shipping regulations and laboratory procedures preferred
- Previous experience with neurological clinical trials and/or PI initiated trials preferred
- Knowledge of research regulations and guidelines, such as ICH/GCP guidelines, Tri-Council Policy, Declaration of Helsinki and FDA CFR and Health Canada TPD
- Ability to perform duties in a professional and courteous manner and produce high quality work while meeting deadlines in accordance to UHN standards
- Exceptional organizational & time management skills & attention to detail
- Ability to multi-task & perform with accuracy in a fast-paced environment
- Well-developed leadership & excellent interpersonal skills
- Self-motivated; ability to work well independently as well as part of a team
- Strong analytical & problem solving skills
- Strong verbal & written communication skills
- Excellent decision-making, listening & conflict resolution skills
- Mentor/training experience an asset
- Proficiency with Microsoft Office Software (Outlook, Word, Excel, PowerPoint)

**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 throughout your career at UHN.
- Competitive offer packages
- Close access to Transit and UHN shuttle service
- A flexible work environment
- Opportunities for development and promotions within a large organization
- Additional perks (multiple corporate discou

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