ICON plc

The Senior Clinical Research Associate will support a study in the cardiovascular/electrophysiology medical device space, requiring monitoring experience and rigorous execution of clinical trial plans. Responsibilities include mitigating risks, identifying site issues, implementing solutions promptly, and maintaining effective relationships with site personnel and internal teams.

The role involves conducting site qualification, initiation, monitoring, and close-out visits for clinical trials while ensuring protocol compliance, data integrity, and patient safety. Responsibilities also include collaborating with site staff, performing data review, and contributing to study documentation preparation and review.

The Senior Clinical System Lead will direct Clinical Data Science project teams through the entire lifecycle of clinical trial systems, including initiation, setup, maintenance, and closing. This role involves supporting business development efforts, performing technical peer reviews, and acting as a primary contact point for internal and external customer teams on assigned studies.

Clinical Operations Lead improving efficiency in oncology clinical trials at ICON plc

The Clinical Scientist assists the CS Protocol Lead and study team with the clinical/scientific conduct of studies, including medical monitoring and managing protocol deviations. They may support multiple studies or lead studies with limited scope, interacting with internal and external stakeholders.

The specialist will support the planning, initiation, and execution of clinical trial activities, including conducting site feasibility assessments and coordinating with investigative sites for protocol compliance. Key duties also involve monitoring study progress and data collection quality, as well as assisting in the preparation and review of study documentation and reports.

Senior Study Manager may lead or support a study or studies, depending on size/complexity. As lead, will be responsible for the following: Operational point of contact for trial execution and all trial deliverables Manages all HQ Operational Activities, including: Establishes, le...

This role involves leading clinical operations for early development oncology projects. Participate as a member of a working group and perform special projects to improve efficiency, effectiveness, and quality of the Development Operations department. Act as preliminary liaison f...

Director Quality Assurance ensuring quality and compliance of clinical trials

Study Manager managing oncology clinical studies for ICON plc