The Contracts Coordinator is responsible for generating company-wide business agreements including Statements of Work, Amendments, and Change Orders. They act as a key resource by collaborating with internal teams such as Business Development, Project Management, and Finance to ensure high-quality contract management.
The Participant Marketing Coordinator manages clinical trial recruitment activities, including social media campaigns, newsletters, and advertising materials. They also ensure compliance with study protocols and GCP while maintaining participant databases and tracking recruitment metrics.
The Executive Director leads HR operations, workforce governance, and people infrastructure to support organizational growth and operational excellence. They partner with senior leadership to drive workforce effectiveness, talent acquisition strategies, and compliance across Canada and the United States.
The Biostatistician II acts as the lead for clinical studies, managing the biostatistics team and ensuring all analysis and documentation comply with regulatory standards. They are responsible for developing statistical analysis plans, generating randomization schedules, and overseeing the quality control of clinical trial data.
The Procurement Specialist I supports sourcing activities for laboratory supplies, raw materials, and equipment while ensuring compliance with regulatory standards like GxP and FDA. They are responsible for processing purchase orders, negotiating contracts, and analyzing spend data to optimize costs and maintain supply continuity.
The Quality Assurance Leader will oversee quality systems, audit programs, and regulatory compliance for early phase clinical research. They are responsible for managing QA staff, identifying risks, and ensuring adherence to GCP and internal SOPs.
The specialist will develop and execute proactive talent attraction and sourcing strategies to build pipelines for scientific, operational, and corporate roles. They will manage a portfolio of requisitions from intake to hire while partnering with hiring managers and marketing to enhance employer branding.
Perform macroscopic and microscopic tissue evaluations and interpret preclinical toxicology studies to diagnose disease or toxicity. Provide scientific leadership, mentorship to staff, and act as a pathology representative for sponsors.
The Veterinary Clinical Pathologist will interpret clinical pathology data and prepare reports for nonclinical safety studies. They will also collaborate with Study Directors and sponsors to address data issues and support scientific initiatives.
