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As a Statistical Programmer II, you will be responsible for the statistical aspects of clinical and preclinical research projects, including study design, analysis planning, and data reporting. You will develop and document SAS programs, assist in protocol implementation, and support statisticians in their tasks while coordinating analysis efforts across multiple projects.
As a Principal, you will lead the Patient Centered Endpoint Intelligence team, providing scientific guidance in endpoint strategy development using Clinical Outcomes Assessments and Digital Health Technologies. Responsibilities include directing data gathering, developing research methodologies, overseeing project deliverables, and mentoring team members.
As a Senior Clinical Research Associate, you will coordinate activities to set up and monitor clinical studies, ensuring compliance with regulations. Responsibilities include managing documentation, preparing regulatory submissions, and potentially mentoring junior CRAs. You'll work closely with a team and travel extensively to monitor study sites.
As a Senior Statistical Programmer, you will lead multi-disciplinary teams, develop and maintain data structures, write standard departmental macros, and train others in data analysis skills, focusing on CDISC ADaM programming.
As a Clinical Research Associate II Specialist, you will conduct site visits for clinical trials, ensure compliance and data integrity, collaborate with staff, resolve data queries, and prepare study documentation. This role is pivotal in advancing innovative medical treatments.
The Senior Financial Accountant will be responsible for financial analysis, reporting, and ownership of project finances. Duties include revenue growth support, financial forecasting, accuracy in reports, external reporting to sponsors, and analyzing financial and operational metrics to assist decision-making within the team.
The Senior QA Auditor will lead and support external audits for ICON, managing CAPA processes and quality issue investigations, ensuring compliance with regulatory requirements, and coordinating with internal and client teams for successful audit outcomes.
The Senior Site Activation Lead is responsible for managing clinical trial start-up activities, overseeing site activation plans, ensuring compliance with project timelines and quality standards, and facilitating effective communication between stakeholders. This role requires strong project management skills and the ability to work collaboratively across various functions and with sponsors.
As a Clinical Research Associate at ICON, responsibilities include setting up and monitoring studies, completing reports, submitting documents for approvals, and ensuring study cost efficiency. Requires at least 12 months of monitoring experience in clinical trials and a college degree in medicine or science.
The InHouse CRA will assist in the planning, initiation, and execution of clinical trials while conducting site feasibility assessments and coordinating with investigative sites. The role involves monitoring study progress and ensuring compliance with protocols and regulatory standards.
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