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Clinical assistant Jobs in Chatham-Kent, ON
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Clinical Research Study Assistant
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- New!
Clinical Neuropsychologist
Hamilton Health Sciences CorporationHamilton, ON, CanadaClinical Research Study Assistant
University Health NetworkToronto, Ontario, Canada- Full-time
Union : Nonunion
Site : Toronto Western Hospital / Schroeder Arthritis Research Institute
Department : Rheumatology
Reports to : Principal Investigator
Work Model : Onsite
Grade : D0 : 03
Hours : 37.5 hours per week
Salary Range : $26.76 $33.45 (to commensurate with experience and consistent with UHN compensation policy)
Status : Temporary FullTime (1 year contract with possibility for extension)
Closing Date : As soon as possible
Position Summary
The Lupus Program at The Centre for Prognosis Studies in Rheumatic Diseases (CPSRD) located at Toronto Western Hospital has a focus on diagnosis treatment and genetic factors of Systemic Lupus Erythematosus (SLE) and has an outstanding tradition of combining scientific rigor with practical relevance. Working under supervision of the principal investigator the Clinical Research Study Assistant will assist in facilitating and coordinating daily study activities and plays a critical role in the conduct of the study.
Duties :
Working under the directions of the Director of the Lupus Program Clinical Research Manager and other senior research staff members the Clinical Research Study Assistant responsibilities include but are not limited to :
- Assist in study participant recruitment by identifying and screening potential subjects obtaining informed consent conducting pretesting and administering questionnaires or other data collection tools.
- Assist in data collection and source documentation following UHN policy and ICH / GCP guidelines.
- Prepare Investigator site file binders as per sponsor policies
- Identify problems using assessment skills and report any abnormalities to the Clinical Research Manager
- Conduct telephone and / or clinical recruitment interviews
- Perform various studyrelated tasks during study visits such as basic administration data collection collecting processing and shipping samples according to the study protocol archiving closeout studies lab kit disposal
- May assist in the preparation of submissions to the Research Ethics Board
- Execute studyrelated administrative tasks including study invoicing and payment tracking and ethics submissions.
Qualifications :
Additional Information :
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.
Current UHN employees must have successfully completed their probationary period have a good employee record along with satisfactory attendance in accordance with UHNs attendance management program to be eligible for consideration.
All applications must be submitted before the posting close date.
UHN uses email to communicate with selected candidates. Please ensure you check your email regularly.
Please be advised that a Criminal Record Check may be required of the successful candidate. Should it be determined that any information provided by a candidate be misleading inaccurate or incorrect UHN reserves the right to discontinue with the consideration of their application.
UHN is an equal opportunity employer committed to an inclusive recruitment process and workplace. Requests for accommodation can be made at any stage of the recruitment process. Applicants need to make their requirements known.
We thank all applicants for their interest however only those selected for further consideration will be contacted.
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