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As a Clinical Research Associate II, you will monitor general medicine trials, ensuring compliance with regulations by coordinating activities, preparing documentation, and mentoring less experienced CRAs. The role involves traveling for site monitoring and maintaining study records in a fast-paced environment.
As a Senior Clinical Research Associate at ICON, you will coordinate and monitor clinical study activities, ensure compliance with regulations, prepare study documentation, and assist in mentorship of less experienced staff. The role involves working with investigational sites and handling sponsor queries efficiently.
As a Study Start Up Associate I, you will facilitate the initiation of clinical trials, ensuring regulatory compliance and supporting study teams in document preparation and coordination with stakeholders.
The Bacteriophage Therapeutics Research Technician II conducts research on phage therapeutics for microbial pathogens, develops phage cocktails for treatment, performs various assays, analyzes experimental results, and maintains laboratory operations and records.
As a Senior Clinical Research Associate at ICON, you will independently coordinate and monitor clinical trials, ensuring compliance with regulations and preparing documentation. You will manage site activities, submit protocols for IRB approval, mentor junior CRAs, and balance sponsor queries while maintaining accurate status reports. Extensive travel is required for site monitoring.
As a Senior Clinical Research Associate at ICON, you will coordinate activities for clinical studies, manage documentation and regulatory submissions, and assist in training other CRAs. You will also be responsible for ensuring compliance with applicable guidelines and effectively balancing sponsor queries. The role involves significant travel and demands excellent communication skills and the ability to produce accurate work under pressure.
As a Senior Clinical Research Associate at ICON, you will coordinate and monitor clinical studies, ensuring compliance with regulations. Your responsibilities include preparing documentation for ethics approval, managing study queries, and possibly training junior CRAs while traveling significantly for site visits.
The CRC Assistant will support Clinical Research Coordinators by assisting with patient visits, documentation, and data management. Responsibilities include performing technical lab procedures, managing quality assurance, entering data in Electronic Data Capture systems, and assisting with various administrative tasks. The role may also involve travel to support clinical studies.
As a Statistical Programmer II, you will manage statistical aspects of clinical and preclinical research, including study design, analysis planning, and data reporting. Responsibilities involve designing and validating SAS programs to generate datasets and summaries, and coordinating analysis across projects.
The Senior Proposals Development Associate will lead the preparation of client-focused proposals and budgets related to clinical trials, coordinating with various internal teams to ensure accuracy and appropriateness for new business opportunities. This role involves evaluating Requests for Proposals (RFPs) and leading budget discussions while maintaining a strong focus on client needs and deadlines.
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