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IntraCare

51 - 200 employees

The current healthcare system is confusing and impersonal. Patients avoid regular checkups because they feel uncomfortable, unheard, or misunderstood. IntraCare seeks to personalize the patient experience by empowering doctors with the resources to give their patients individualized attention. The need to be healthy is one of the few things we all have in common. The system by which we administer and receive healthcare should reflect that unity. IntraCare helps connect patients, doctors, and medical programs to provide people-focused healthcare.Many providers can relate to healthcare as a battlefield. Providers find themselves caught between competing priorities and needs. Although providers enter the healthcare field passionate about their work, they are soon obstructed by the details of owning an independent practice. IntraCare simplifies the patient care process and empowers providers to do what they love. By partnering with us in creative, highly aligned ways, IntraCare will increase the quality of service and accessibility in our partners’ communities. As we build on ten years of excellence in value-based care and connect with a high-quality network of over 200 experienced providers, we will manage an excellent system of care that is inclusive and integrated to help patients across the nation. Everyone deserves access to accessible and affordable healthcare regardless of race, religion, nationality, or financial status. We want to advance the health industry by partnering with physicians to provide personalized, intentional care in communities that have been overlooked.

πŸ“‹ Description

β€’ Provide operational leadership and quality oversight across clinical research sites. β€’ Train, onboard, and mentor Clinical Research Coordinators and research staff. β€’ Develop and maintain standardized workflows, SOPs, and best practices across sites. β€’ Review source documentation, regulatory files, and study data for completeness, accuracy, and protocol compliance before submission. β€’ Ensure compliance with study protocols, ICH-GCP guidelines, sponsor requirements, and internal SOPs. β€’ Support regulatory document preparation and maintenance of essential study files. β€’ Assist sites with audit readiness, monitoring visit preparation, and corrective action implementation. β€’ Provide ongoing education and retraining to research staff as protocols and processes evolve. β€’ Monitor research quality metrics and identify opportunities for operational improvement. β€’ Collaborate with investigators, site leadership, sponsors, and operations to maintain high-quality research standards.

🎯 Requirements

β€’ Experience in clinical research operations. β€’ Strong understanding of ICH-GCP, FDA regulations, and clinical trial processes. β€’ Experience with regulatory documentation and sponsor requirements. β€’ Excellent organizational, leadership, and communication skills. β€’ Ability to train, mentor, and develop research personnel. β€’ Experience with CTMS, EDC, eSource, and electronic regulatory systems preferred.

πŸ–οΈ Benefits

β€’ Health insurance β€’ Paid time off β€’ Flexible work arrangements β€’ Professional development opportunities

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