CRIO
CRIO is a company that provides an all-in-one platform for clinical research operations, focusing on improving protocol compliance, eliminating transcription tasks, and saving time and money for sites and sponsors. CRIO's solutions support single sites, networks, academic research, and sponsors, offering products like eSource, eConsent, medical record APIs, and site CTMS, among others. The company emphasizes innovation, collaboration, and efficiency, with tools that enhance clinical trial site operations and promote diversity in clinical research. CRIO partners with other companies to drive innovation within the industry, and their platform is widely used for its reliability and ease of use in clinical settings.
Clinical Trial Research Studies • Data Management • Electronic Data Capture (EDC) • eSource • CTMS
Study Design Specialist
November 5, 2024
CRIO
CRIO is a company that provides an all-in-one platform for clinical research operations, focusing on improving protocol compliance, eliminating transcription tasks, and saving time and money for sites and sponsors. CRIO's solutions support single sites, networks, academic research, and sponsors, offering products like eSource, eConsent, medical record APIs, and site CTMS, among others. The company emphasizes innovation, collaboration, and efficiency, with tools that enhance clinical trial site operations and promote diversity in clinical research. CRIO partners with other companies to drive innovation within the industry, and their platform is widely used for its reliability and ease of use in clinical settings.
Clinical Trial Research Studies • Data Management • Electronic Data Capture (EDC) • eSource • CTMS
📋 Description
• Who We Are: • CRIO (Clinical Research IO) is a health tech company helping pharma, biotech, research sites, and academic research centers streamline regulatory workflows. • CRIO’s eSource and CTMS system is a leading, modern platform for clinical research. • In 2022, CRIO released its Reviewer product, allowing for thorough data review in eSource. • The Study Design Specialist creates comprehensive study builds from start to finish in the CRIO platform. • Responsibilities include developing eSource from protocols, conducting quality control reviews, and mentoring. • Join us at CRIO and be part of a dynamic team dedicated to revolutionizing the clinical research industry.
🎯 Requirements
• Utilize protocols, eCRF guidelines, pharmacy manuals, lab manuals, and other source documents to produce comprehensive builds for clients. • Complete client-requested edits and customizations. • Manage complex trials to ensure all data is captured appropriately. • Modify standard templates to comply with protocol requirements. • Complete assignments on time. • Mentor and train current and new CRIO employees. • Experience with eSource and QC design in CRIO or other eSource/CTMS systems. • BS in medical or sciences field. • Experience as a Research Coordinator, Site Director, or Source Designer is a plus. • At least 1 year of healthcare experience. • Ability to interpret clinical trial protocols, and source documents. • Knowledge of medical terminology and procedures. • Strong people skills. • Detail-oriented with solid time management skills. • Well-organized, capable of establishing priorities, and executing tasks efficiently.
🏖️ Benefits
• This is a part time role: • Compensation Package - $20 an hour for all training and up to $450 for Study Design Build
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