132 - Clinical Trials Recruitment Specialist

3 weeks ago

Winnipeg, Canada CancerCare Manitoba Full time

**Clinical Trials Recruitment & Quality Facilitator**
**Clinical Trials Unit - MacCharles**

**Permanent, Full-time (1.0 EFT)**
Competition #: 132-23-762111537

**Job Summary**:
Reporting to the Clinical Trials Unit (CTUs) Resource Coordinator, Ethics & Regulatory Affairs, the Clinical Trials Recruitment & Quality Facilitator is responsible for both trial recruitment activities and the quality aspects of clinical trials. In the recruitment role, the incumbent is responsible for coordinating all aspects of screening and recruitment to CTU clinical trials. In the quality role, the incumbent leads audits and inspections and works to address issues related to protocol violations, policy and procedure and standard operating procedures. The incumbent will complete quality audits, study risk assessments, create monitoring plans and monitor trials where CCMB is the sponsor.

**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
- Minimum 5 years’ clinical trials experience
- Certification in clinical research (i.e. SoCRA) or willing to obtain certification within 2 years of employment
- Proficiency in Microsoft Office, including the creation of graphs and charts
- Satisfactory employment record
- Must be able to legally work in Canada
- To be determined during the interview process:_
- Excellent knowledge of anatomy and physiology and interpreting complex medical reports
- In depth knowledge of clinical trial regulations
- Self-directed and demonstrated ability to take initiative
- Demonstrated professional and ethical behaviour in the workplace
- 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 excellent work record
- Demonstrated attention to accuracy and detail
- Demonstrated positive attitude and is a positive role model for other staff

**Preferred**:

- Experience as a Clinical Research Professional or Clinical Research Professional in Ethics & Regulatory Affairs
- Demonstrated proficiency with electronic patient records (i.e. ARIA)

**Asset**:

- Clinical trials experience in oncology
- Experience leading and making presentations to groups, public speaking
- Bilingual (French/English) written and verbal skills

**Salary**: As per CUPE collective agreement

Please submit a detailed cover letter outlining how you meet the requirements for this position along with a current resume which references the Competition Number

**Closing Date**: May 4, 2023

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