Clinical Research Professional
3 weeks ago
**CancerCare Manitoba** is a provincial agency which provides clinical and academic services and leadership for cancer control and the treatment of blood disorders. Our shared vision of a **world free of cancer** drives every member of our team. CancerCare Manitoba is the perfect place to thrive if you're seeking a fulfilling career in an organization that is committed to its employees' well-being and professional development.
**Competition # 357-23-762081092**
**Posting End Date: November 14, 2023**
**City**:Winnipeg
**Work Location**:MacCharles
**Department**:Clinical Trials Unit
**Union**: CUPE FS
**Hiring Status**: Permanent
**Anticipated Start Date**:ASAP
**FTE: 1.0**
**Anticipated Shift**:days
**Daily Hours Worked**:7.5
**Annual Base Hours**:1950
**Salary**:$27.705 /$28.270 /$28.849 /$29.438 /$30.037 /$30.610
**Job Summary**:
Reporting directly to the Resource Coordinator, Ethics & Regulatory Affairs (ERA RC), the ERA CRP functions as an essential member of the clinical research team and is responsible for actively ensuring all clinical research team members adhere to all institutional, provincial, national and international guidelines and regulations for the conduct of clinical trials. The ERA CRP is responsible for preparing and coordinating the initial and continuing ethics, scientific and operational review and regulatory management of clinical trials run through the Clinical Trials Unit at CancerCare Manitoba. The ERA CRP must ensure the appropriate dissemination of study and regulatory information to all clinical research team members and maintain standards 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 post-secondary education in a health care field plus research-related experience may be considered
- Proven analytical and problem-solving skills
- Proficiency in Microsoft Office and Internet
- Excellent employment record
- Must be able to legally work in Canada
- 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
- Evidence of excellent communication (oral, written and listening), organization and problem solving skills
- Demonstrated attention to accuracy and detail
- Demonstrated professional and ethical behaviour in the workplace
- Preferred:_
- Clinical research experience
- Ethics and regulatory affairs experience
- Experience working in oncology
- Certification in clinical research (e.g. SoCRA or ACRP)
- Asset:_
- Experience working or volunteering in a health-care environment
- Ability to speak French
Interested and qualified applicants are invited to submit a detailed and current resume, plus a cover letter demonstrating how you meet the above qualifications and the above competition number.
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