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The Senior Clinical Research Associate will monitor clinical studies, ensuring compliance with protocols, regulations, and procedures, while also overseeing remote and on-site clinical trial progress.

The Global Study Manager prepares study documents, manages study interactions, ensures compliance with regulations, supports budget management, and maintains project oversight with vendors.

As a Clinical Research Associate, you'll monitor clinical trials, ensure protocol compliance, collaborate with site staff, and maintain data integrity.

The Clinical Research Associate will coordinate clinical trials, ensuring compliance, collecting data, and maintaining study documentation while fostering relationships with stakeholders.

The Contract Analyst II will review, analyze, and negotiate contracts and agreements related to clinical trials, collaborate with teams on contract risks, and provide guidance on compliance and dispute resolution.

As a Contract Analyst II, you will review and analyze contracts related to clinical trials, negotiate terms, collaborate with teams, and provide guidance on contract matters.

The Clinical Trial Coordinator manages trial and site administration, document management, regulatory duties, budgeting, and meeting planning to support clinical research operations.

As a Senior Clinical Research Associate, you will monitor clinical studies, ensuring compliance with protocols and regulatory requirements. You will work both on-site at investigative sites and remotely, focusing on data integrity and patient safety.

As a Clinical Research Associate II, you will conduct site visits, ensure protocol compliance, maintain data integrity, and prepare study documentation.

As a Senior Clinical Data Science Lead, you will lead clinical data management strategies, oversee data analysis for trials, and guide teams in data governance and quality control.