The Clinical Research Coordinator II independently manages clinical research studies involving human subjects, including patient screening, informed consent, and data collection consistent with regulatory requirements. This role emphasizes collaboration with medical personnel and regulatory bodies to ensure compliance with FDA and IRB standards while advancing research in digital health and cancer survivorship. The position requires strong data management skills, experience with statistical software, and is 100% onsite to support team-based research activities and participant engagement.
The top qualifications for success in this role include hands-on experience coordinating clinical research involving human subjects, including familiarity with IRB processes, informed consent, and direct or virtual patient engagement. Additionally, applicants should bring strong data analysis and management skills, ideally with experience working with clinical or digital health data, statistical software (e.g., R, Stata, SAS), and tools like REDCap.
This is an exciting opportunity for medical students to contribute to innovative research at the intersection of digital health and cancer survivorship. Participants will gain meaningful experience through patient interaction, data-driven research, and collaborative scholarly activities—with opportunities to support abstract submissions, manuscripts, and interdisciplinary projects that advance the field.
The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for accurate and timely source documents, data collection, documentation, entry, and reporting including timely response to sponsor queries. Responsible for compiling and reporting on each study including information related to protocol activity, accrual data, workload, and other research information. Presents information at regular research staff meetings. May plan and coordinate strategies for increasing patient enrollment, improving efficiency, training of personnel, or identifying new research opportunities. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board (IRB).
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.
Primary Duties and Responsibilities
The top qualifications for success in this role include hands-on experience coordinating clinical research involving human subjects, including familiarity with IRB processes, informed consent, and direct or virtual patient engagement. Additionally, applicants should bring strong data analysis and management skills, ideally with experience working with clinical or digital health data, statistical software (e.g., R, Stata, SAS), and tools like REDCap.
clinical research, clinical trials, patient screening, informed consent, data management, IRB compliance, FDA regulations, digital health, cancer survivorship, statistical software
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