Support efforts to define, adopt, and oversee compliance to processes and standards related to technology solution development, validation, and delivery.
Monitor, identify, and implement continuous process improvement across technology platforms impacting clinical research.
Provide expertise to ensure technology solution projects adhere to established standards and quality expectations including validation, access control, audit trail reviews, system reviews.
Supports activities to develop and perform assessments on technology solution projects which are low or medium regulatory risk systems to identify and mitigate risks and prevent quality concerns.
Support monitoring and maintenance of oversight for the selection and implementation of technology platforms for quality management in support of delivery of products and services.

QUALIFICATIONS

• The successful candidate will possess either an undergraduate degree with 1-3 years of related experience and ongoing training, or a College Diploma with 4-6 years of related experience and training.
• Entry/mid-level experience in computer technology, quality and compliance (including computer system validation) and clinical research is preferred.
• Analytical, critical thinking, problem solving and attention to detail skills required.
• Knowledge of ICH GCP and global regulations governing technology platforms in clinical research is required.
• Basic knowledge of continuous improvement methodologies.
• Excellent interpersonal, verbal, and written communication skills as well as business understanding.

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• Accommodations for applicants with disabilities are available upon request throughout the recruitment lifecycle

Please refer the Job description for details