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The role involves leading regulatory CMC strategy for peptide and oligonucleotide therapeutics, driving submissions, and ensuring compliance with relevant standards.

The Sr. Clinical Research Associate manages and monitors clinical trials, ensuring compliance with regulations, patient safety, and quality delivery at sites.

The role involves designing, developing, and maintaining Power BI reports, collaborating with stakeholders, analyzing requirements, and optimizing SQL queries for comprehensive insights.

Manage clinical trial budgets and contracts, ensuring compliance with regulations while collaborating with stakeholders and solving complex financial issues.

The Senior CRA ensures quality site management and monitoring of clinical trials, addressing protocol-related issues while maintaining compliance and investigator relations.

Lead and coordinate global labeling initiatives, ensuring compliance with regulatory requirements. Manage label governance and support product lifecycle management across multiple markets.

The Manager, Data Analysis oversees centralized monitoring for clinical trials, ensuring effective RBQM systems, data analysis, and reporting while collaborating with cross-functional teams.

The Clinical Business Liaison manages clinical trial budgets and contracts, ensuring compliance with regulations, optimizing financial aspects, and collaborating with multiple stakeholders.