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Become a Site Activation Coordinator, ensuring smooth operations and compliance in clinical studies from initiation to closure.Bring your expertise in study start-up to the forefront.As a Site Activation Coordinator, you will manage and support operational tasks for clinical studies effectively.This

Elevate your career as an Operations Manager for Clinical Trials at Parexel, where you will oversee vital study activities across various regions. Key Responsibilities: - Supervise study execution and local study teams - Liaise with pCROs to ensure quality deliverables - Drive recruitment strateg

Become a Site Activation Specialist, ensuring successful startup and operations for clinical trials.This role focuses on compliance with client standards and efficient document management.As the Site Activation Specialist, you will lead the coordination for assigned studies from start to finish, act

The Site Activation Partner is responsible for leading or supporting operational activities from startup to close‑out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Client standards.Clinica

The Site Activation Partner is responsible for leading or supporting operational activities from startup to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Client standards.Clinical

Consent, eISF, remote source access, remote source data verification/review (SDV/SDR), iConnect, implementation of protocol required decentralized trial options) Compliance with Parexel Standards Complies with required training curriculum Completes timesheets accurately as required Submits expe

Compliance with Parexel standards. Maintains a working knowledge of and complies with Parexel processes, ICH-GCPs and other applicable requirements.

When our values align, there's no limit to what we can achieve.Remote - ALL Canada Locations- Oncology experience preferred.The Senior Clinical Research Associate (Sr.CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure p

When our values align, there's no limit to what we can achieve.The Senior Clinical Research Associate (Sr.CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with

Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs; as applicable) and liaising wit