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.

The Clinical Site Associate will manage site-level communications, coordinate trainings, support site readiness activities, and follow up on action items. Responsibilities also include maintaining accurate documentation within the Trial Master File (TMF).

The Senior Clinical Trial Manager will be responsible for ensuring the successful delivery of all clinical aspects of studies, including overseeing the clinical portion of the budget and developing effective monitoring plans. Key duties involve driving enrollment, leading study start-up activities, training CRAs, reviewing trip reports, and fostering productive relationships with sponsors and cross-functional teams.

The Senior Clinical Data Science Lead will lead the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting across studies. This role involves overseeing clinical data analysis to provide actionable insights and providing strategic guidance on data governance and regulatory compliance.

The moderator will collaborate with subject matter experts to define presentation objectives and design visually engaging presentations using PowerPoint or other software, incorporating graphics and multimedia elements. They will also develop templates, provide guidance on best practices for delivery, and manage projects to meet deadlines.