046 - Clinical Research Professional - Ethics &

7 days ago

Winnipeg, Manitoba, Canada CancerCare Manitoba Full time

Ethics & Regulatory Affairs Clinical Research Professional, Level 11

Clinical Trials Unit - St.
Boniface

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

Competition # /

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 postsecondary education in a health care field plus researchrelated experience may be considered
  • Proven analytical and problemsolving skills
  • Proficiency in Microsoft Office and Internet
  • Excellent employment record
  • Must be able to legally work in Canada
  • Must have a valid passport to participate in National Cancer Institute (NCI) US funded studies or willing to 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
  • 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

Will be assessed during the testing process:

  • Written communication skills
  • Grammar
  • Attention to detail
  • 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 healthcare environment
  • Ability to speak French

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:
February 21, 2023

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