The Company: NeuroRx is a leader in advanced brain image analysis and project management servicing the pharmaceutical and biotech industry. We are involved in all MRI-related activities in the context of clinical trials in neurology, phases 1 through 4. Please visit our website at www.neurorx.com. The role: The Quality Assurance / Quality Control Coordinator is part of NeuroRx\xe2\x80\x99 QA Unit and is responsible for internal Quality Assurance (QA) monitoring activities as well as for Quality Control (QC) of MRI related data in our database. Duties of the Quality Assurance / Quality Control Coordinator include:
QC of quantitative measurement results in database against source documents prior to scheduled data transfers
Review of trial-specific paper and electronic documentation for accuracy and completeness
Internal trial-specific audits to ensure that trial management and image analysis are conducted in accordance with study protocols, ICH-GCP, the applicable regulations, and NeuroRx SOPs
Internal audits of NeuroRx Systems to ensure that company operations and documentation are in compliance with ICH-GCP, the applicable regulations, and NeuroRx SOPs
Facilitating the Reader QA Program
Following up on CAPA plans
The Quality Assurance / Quality Control Coordinator is overseen by, and reports to the QA Unit Manager. This is a full time position, and there is a probation period of 6 months. Requirements: Education- A bachelor\xe2\x80\x99s degree Language- Excellent oral and written English We are looking for candidates who are:
Detail oriented (attention to detail is an absolute requirement)
Dynamic
Professional
Efficient
Organized
Accountable
Team player
Able to express oneself in a clear, concise manner, verbally and in writing (good communication skills is key to working well within the team and inter-departmentally, on a daily basis)
Able to function under pressure and handle multiple deadlines at once
Able to multitask and thrive in a fast paced environment
Experience in Quality Assurance, Quality Control and/or clinical trials is an asset. An understanding of Good Clinical Practices is also an asset. Submitting your CV: **** All CV\xe2\x80\x99s must be accompanied by a cover letter (which includes why you would be a good fit, your mid/long-term goals, and salary expectations). Applications for which the cover letter does not include those requirements will not be considered. Please DO NOT CALL . Only selected candidates for a first interview and tests will be contacted. ** Only candidates with the valid work permit to work in Canada should apply!**ALL successful applicants will be required to undergo a background check.** Job Type: Full-time
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