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The Sub-Investigator will support clinical research studies, overseeing execution of study protocols, administering investigational products, monitoring reactions, and ensuring compliance with regulations. They will work both remotely and in-person with study subjects, perform physical examinations, and maintain communication with internal teams and investigators.
The QMS Coordinator will manage and improve the Quality Management System (QMS), ensuring compliance with ISO and GCP standards. Responsibilities include maintaining QMS documentation, facilitating staff training, monitoring compliance timelines, performing system administration, and reporting on QMS performance.
The Operational Compliance Specialist leads operational quality compliance, conducts compliance checks on clinical trial documents, maintains quality support for regulatory compliance, and facilitates process improvement and CAPA management to enhance operational effectiveness and business success.
The Sub-Investigator will oversee clinical study protocols, ensuring compliance with regulatory standards and managing study subjects' medical issues during visits. Responsibilities include reviewing documentation, reporting adverse events, and conducting physical examinations. This role involves regional travel and telemedicine work.
As a Data Engineer, you will maintain and optimize the data architecture by designing and implementing data platforms and pipelines, supporting migrations, troubleshooting issues, and ensuring compliance with regulations. You will also address stakeholder requirements and provide training support to staff members.
The IT System Administrator will support daily IT operations by managing accounts, devices, and network systems, as well as designing and implementing necessary IT assets. They will ensure compliance with security standards while training users and documenting IT processes.
The Senior Director of Contracting oversees the contracting ecosystem at Care Access, leading the contracting team and collaborating with various departments to ensure compliance. Responsibilities include negotiating critical agreements, implementing improvements to contracting processes, and setting KPIs to enhance efficiency and effectiveness in contracts management.
The Study Activation & Readiness Specialist will manage study readiness activities, ensuring compliance and regulatory requirements are met for clinical trials. Responsibilities include effective communication with stakeholders, document management, supporting audits, providing training on various systems, and optimizing processes within the department.
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