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Clinical Research Assistant, TFT, Cancer Centre, #18-0848

Internal Job Posting #18-0848
*REPOSTED*
*Approximately 1 year or until the previous incumbent returns*
Temporary Full Time Clinical Research Associate -  Cancer Centre

DEPT

Cancer Centre

#POSITIONS

1

PROGRAM

Regional Cancer Program

UNION GROUP

Non Union

HOURS

Days

SALARY RANGE

As per pay scale


 
POSTED: August 10, 2018                                                       CLOSE DATE: August 17, 2018
 

Job Summary:
The Clinical Research Assistant is responsible for the organization, co-ordination and ongoing conduct of assigned clinical research trials.  This person will prepare, and collect required documentation across the continuum of all Clinical Research studies while ensuring accurate, concise and timely submission of documentation to sponsoring Canadian, American and International agencies.
 
Required Qualifications:
Post Secondary education in a Health Science field of study is required
Bachelor of Science (BSc.) preferred
Clinical Research Associate Certificate required
National Institute of Health (NIH) research participants Web course preferred
2 years related experience, in a clinical research setting, or equivalent combination of education and experience.
2 years’ experience in clinical research conducting clinical trials, registering eligible patients , and interacting with patients and their families following patient-centered care model.
2 years’ experience explaining details and requirements of the trial design to patients and or family.
Advanced knowledge of the current regulatory environment in Clinical Research
             FDA – Code of Federal Regulations
             FDA Audit procedures
             Privacy legislation
             Health Canada Clinical Trial Applications (CTA)
             Health Canada inspections procedures
             Health Canada Food & Drug regulations
             Tri-Council Policy
Understands the objectives of the clinical trials currently open to accrual and demonstrates knowledge of all active and inactive protocols at the Centre.
The ability to read test results (i.e. pathology, radiology, cytology, biochemistry) and identify appropriate medical reports.
Knowledge related to CRF,eCRF, PRO and ePRO,completion and ethics/regulatory submissions.
Demonstrates ability to prioritize workload, with particular attention to detail.
Proficient in MS Windows environment (Word, Excel, Power Point).
Relevant clinical trials and/or oncology experience preferred.
Working knowledge of computers and data entry experience.
Demonstrates excellence in communication, both written and verbal
Analysis / problem assessment
Innovative and willing to learn
Demonstrates individual leadership skills
 
At Southlake Regional Health Centre, we are committed to fostering an inclusive and accessible environment.  We are dedicated to building a workforce that reflects the diversity of the community in which we live and serve, including those with disabilities.  Southlake Regional Health Centre is committed to providing accommodations in all parts of the hiring process.  If you require an accommodation, we will work with you to meet your needs.
 
It is the responsibility of all Southlake Regional Health Centre employees to work in a safe manner and promote health and safety in the workplace

 

Southlake Regional Health Centre
596 Davis Drive, Newmarket, Ontario   L3Y 2P9
Tel: 905-895-4521   |   TTY: 905-952-3062
Copyright © 2012 Southlake Regional Health Centre
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