044 - Clinical Research Professional

1 month ago

Winnipeg, Canada CancerCare Manitoba Full time

**Clinical Research Professional - Level 10**

**Clinical Trials Unit - MacCharles**

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

Competition #: 044-23-762111537/762081091/762081093

**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 post-secondary 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 multi-disciplinary team
- Demonstrated ability to multi-task and work under pressure while meeting multiple deadlines
- Demonstrated ability to organize and problem-solve
- 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 health-care environment
- Ability to speak French

**Salary**: As per CUPE Collective Agreement

**Closing Date**: February 21, 2023

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