The Clinical Research Specialist II at the Clinical Coordinating Center (CCC) manages and coordinates investigator-initiated and multi-site clinical research projects. This role involves design, implementation, regulatory compliance, and communication with internal and external stakeholders to ensure quality and adherence to federal and local regulations. The position is fully onsite and requires expertise in clinical research, protocol development, and research infrastructure management.
This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time.
Within ACRO, the Clinical Coordinating Center (CCC) offers infrastructure and expertise for investigator-initiated trials (IITs) and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional role and interface with internal and external stakeholders to coordinate all aspects of assigned investigator-initiated and multi-site projects.
The Clinical Research Specialist II provides clinical research expertise by participating in the design and implementation of research projects as needed. Responsible for specific and assigned aspects of research infrastructure development, coordinates projects, and communicates status and improvement areas to leadership. May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
Primary Duties and Responsibilities
This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time.
Requirements:
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Req ID : 8229clinical research, investigator-initiated trials, multi-site projects, regulatory compliance, protocol development, clinical trial recruitment, FDA regulations, IRB compliance, Good Clinical Practice, research coordination
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