Lead and execute assigned clinical trials end-to-end: develop operational plans, manage cross-functional teams and CROs, track milestones and budgets, ensure GCP/ICH compliance, maintain TMF and inspection readiness, provide monitoring oversight, support global regulatory submissions, report to senior management, mentor study staff, and drive process improvements.

The Sr. Regulatory Affairs Specialist will manage regulatory filings, ensure compliance with FDA and Canadian regulations, develop strategies for submissions, and coordinate cross-departmental communications related to regulatory affairs.

The Research Associate prepares sequencing chemistry reagents, supports instrument operations, manages inventory, and collaborates within a multidisciplinary team.