044 - Clinical Research Professional - Winnipeg, Canada - CancerCare Manitoba

CancerCare Manitoba

Verified Company

Winnipeg, Canada

1 week ago

Posted by:

Sophia Lee

beBee Recruiter

Description

Clinical Research Professional - Level 10

Clinical Trials Unit - MacCharles

Permanent, Full-time (1.0 EFT) - Grant Funded

Competition #:
/ /

Job Summary:

Reporting directly to the Resource Coordinator, the Clinical Research Professional (CRP) functions as a member of the clinical research team and is responsible for actively ensuring adherence to the study protocol through the interpretation and abstraction of complex health information related to a patient's participation in an oncology and or benign hematology clinical trial at CancerCare Manitoba (CCMB) (outpatient) and Health Sciences Center (inpatient).

Maintains comprehensive clinical trial patient and study files and communicates effectively with study sponsor representatives. Participates in the accomplishment of CCMB organizational goals and trials office objectives. Maintains standard of excellence in clinical trial management. Overtime and flexibility to move between CCMB locations may be required. *_aka: Study Coordinator / Clinical Research Associate._

Qualifications:

Required:_
Health Information Technologist/Health Information Management Diploma or an equivalent combination of postsecondary education in a health care field plus clinical research experience may be considered
Must have a satisfactory employment record
Must be able to work legally in Canada
Must have a valid passport to participate in National Cancer Institute (NCI) US funded studies or willing or obtain within 2 months of hire
Will be assessed during the interview process:_
Demonstrated ability to work effectively, both independently and as a member of a multidisciplinary team
Demonstrated ability to multitask and work under pressure while meeting multiple deadlines
Demonstrated ability to organize and problemsolve
Excellent communication skills in English (oral and listening)
Demonstrated proficiency in Microsoft Office
Demonstrated attention to accuracy and detail
Demonstrated professional and ethical behaviour in the workplace
Will be assessed during the testing process:_
Written communication skills
Grammar
Attention to detail
Preferred:_
Clinical research experience with the adult population
Health Information Technologist/Health Information Management Diploma
Certification in clinical research (e.g. SoCRA, ACRP)
Asset:_
Experience working with clinical trials
Experience working or volunteering in a healthcare environment
Ability to speak French