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Cancer Research Monitor/Auditor - Kingston, Canada - Queen's University
Description
About Queen's University
Queen's University is the Canadian research intensive university with a transformative student learning experience. Here the employment experience is as diverse as it is interesting. We have opportunities in multiple areas of globally recognized research, faculty administration, engineering & construction, athletics & recreation, power generation, corporate shared services, and many more.
We are committed to employment equity and diversity in the workplace and welcome applications from individuals from equity seeking groups such as women, racialized/visible minorities, Indigenous/Aboriginal peoples, persons with a disability, persons who identify in the LGBTQ+ community and others who reflect the diversity of Canadian society.
Come work with us
Job Summary
Under the supervision of the Compliance Group (CG) Team Leader, the Cancer Research Monitor/Auditor will conduct quality control and assurance activities for clinical trials in North America, providing support to both the monitoring and audit programs of the Canadian Cancer Trials Group (CCTG), as required.
The Cancer Research Monitor/Auditor will also participate in other compliance activities including, but not limited to, involvement with the Centre Performance Index (CPI) and Online Information Organization Network (ONION), and participation on committees and training programs critical to compliance assurance. The incumbent will also participate in central office data review, assessment, and querying procedures as needed.
Job Description
KEY RESPONSIBILITIES:
•Apply an understanding of clinical trials methodology, data collection and analysis, and cancer biology diagnosis and treatment in order to contribute to the oversight and review of multi-centre clinical trials in cancer therapy and supportive care.
•Coordinate and participate in quality control and assurance activities with participating member centres (cancer treatment centres), vendors, and collaborators, as well as internal trial teams, in order to ensure compliance.
•Interpret findings and identify issues such as non-compliance or scientific misconduct and notify CCTG personnel as needed. Ensure appropriate corrective action is undertaken for any identified deficiencies.
•Coordinate and participate in external audits and/or regulatory inspections in support of the overall quality control and assurance program of the CCTG.
•Apply an understanding of the current computer systems and applications in clinical trials conduct to effectively conduct compliance activities (e.g. EDC Medidata Rave). Provide education to participating member centres during on-site reviews and liaise internally to ensure trial standards.
•Promote awareness and understanding of Good Clinical Practice and other appropriate compliance procedures and guidelines. Act as a representative of CCTG in interactions with member centres, while conducting on site monitoring visits.
•Delegate work to AMG Assistants and ensure its completeness and accuracy. Participate in the training and mentoring of new monitors/auditors and others.
REQUIRED QUALIFICATIONS:
•Master's degree in Health Sciences or equivalent combination of education and experience in a medical, research or pharmaceutical setting.
•Minimum of 2-3 years relevant experience in one or more of the following: clinical research, clinical trial methodology, quality assurance, monitoring.
•Consideration may be given to an equivalent combination of education and experience.
SPECIAL SKILLS:
•Respect diversity and promote inclusion in the workplace.
•Excellent organizational skills.
•Attention to detail.
•Superior communication skills both written and verbal.
•Ability to work independently and liaise effectively in a cooperative spirit with colleagues both within the central office and across the country.
•Ability to prioritize competing demands.
•Ability/enthusiasm to learn new skills.
•Proactive, consultative, and collaborative.
•Proven problem solving and analytical skills.
•Understanding of IT systems capabilities including evolving electronic data capture systems (e.g. Medidata Rave).
•Computer skills including WORD, Excel, Oracle.
•Working knowledge of French is an asset.
•Ability to travel in North America approximately 60% time.
DECISION MAKING:
•Interpret findings and identify issues such as non-compliance or scientific misconduct and notify CCTG personnel as needed.
•Determine and ensure implementation of appropriate corrective action required to resolve any identified deficiencies.
•Independent, ongoing assessment of workload priorities is essential to integrate the overall organization, day-to-day administration, and medical review of data and analyses of many trials.
•Participate in ongoing review of CCTG SOPs to ensure optimal methods to assess compliance are in place, assure consistency across Compliance.
•Oversees, delegates and assesses the quality of work of the AMG Assistants, and recommends need for formal training or development plans and identifies possible staff performance and/or disciplinary issues to Team Leader.
Employment Equity and Accessibility Statement
The University invites applications from all qualified individuals. Queen's is committed to employment equity and diversity in the workplace and welcomes applications from women, visible minorities, Aboriginal Peoples, persons with disabilities, and persons of any sexual orientation or gender identity. In accordance with Canadian Immigration requirements, priority will be given to Canadian citizens and permanent residents.
The University provides support in its recruitment processes to applicants with disabilities, including accommodation that takes into account an applicant's accessibility needs.
