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CLINICAL RESEARCH COORDINATOR
CLINICAL RESEARCH COORDINATORDuke Clinical Research Institute • Durham, NC, United States
CLINICAL RESEARCH COORDINATOR

CLINICAL RESEARCH COORDINATOR

Duke Clinical Research Institute • Durham, NC, United States
19 days ago
Job type
  • Full-time
Job description
School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,500 faculty physicians and researchers, more than 1,300 students, and more than 6,000 staff, the Duke University School of Medicine along with the Duke University School of Nursing, Duke University Health System and the Private Diagnostic Clinic (PDC) comprise Duke Health. a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Primary Care, Duke Home and Hospice, Duke Health and Wellness, and multiple affiliations.

Position Overview

Supports day-to-day execution of complex human subject studies with a primary focus on hands-on data collection, wearable device deployment, and participant support. Coordinates participant scheduling, study visits, and longitudinal in-clinic and at-home protocols. Conducts study visits including fitting, configuring, deploying, and troubleshooting wearable technologies (e.g., physiological sensors, mobile/cloud apps, eye tracking, activity and sleep monitoring). Supports studies involving participants with chronically implanted electrodes or neurostimulation devices, including coordination of passive iEEG data collection and alignment of implanted, wearable, and behavioral data. Develops and maintains SOPs for device deployment, data capture, synchronization, troubleshooting, and participant training. Monitors adherence, identifies and resolves technical issues, and collaborates with engineering, data science, and clinical teams as needed. Supports regulatory activities (IRB, FDA, agreements) in collaboration with the PI and institutional offices.

Participant Interaction & Safety

Conducts and documents informed consent for complex technology-enabled studies, clearly explaining wearable data collection, implanted device recordings, and at-home procedures. Monitors and documents adverse events and participant-reported issues related to devices or study procedures and communicates concerns to the PI and study team.

Data Collection & Data Quality

Leads multimodal data collection across wearable sensors, mobile applications, cloud systems, clinical sources, and implanted neurodevice recordings. Ensures accurate and complete longitudinal data capture through real-time quality monitoring, troubleshooting data loss, and documenting technical issues. Develops and maintains SOPs for data synchronization, storage, transfer, and quality assurance. Works closely with data scientists and investigators to flag missing or anomalous data and prepares summaries and reports on data completeness, adherence, and study progress.

Protocol Development & Scientific Support

Contributes to protocol development with attention to feasibility, participant burden, and real-world deployment of wearable and implanted sensing technologies. Assists with scientific presentations and publications, particularly methods and data-collection sections.

Operational Coordination

Coordinates study visits with an emphasis on device readiness, equipment functionality, and longitudinal data collection. Manages participant schedules and tracking of wearable data capture milestones and flags protocol deviations. Ensures studies are conducted in compliance with institutional requirements while prioritizing participant experience.

Study Execution & Team Collaboration

Demonstrates ownership of study execution and data workflows. Proactively identifies and resolves issues related to participant experience, device performance, or data quality. Communicates effectively across multidisciplinary teams and serves as a reliable point of contact for participants in technology-enabled studies. Adapts to evolving protocols and emerging technologies and contributes to continuous improvement of SOPs and best practices.

Laboratory Overview

The Suthana Laboratory conducts human neuroscience research integrating intracranial electrophysiology, wearable sensing, and real-world behavioral measurements to study memory, emotion, and neuropsychiatric disorders, with both in-lab and at-home data collection.

Experience Requirements

Experience working directly with human research participants in device-based or technology-heavy studies.
Comfort troubleshooting wearable sensors, mobile apps, and data capture systems.
Experience with clinical populations and/or participants with implanted neurodevices preferred.

Anticipated Pay Range:

Duke Universityprovides an annual base salary range for this position as USD $59,829.00 to USD $99,960.00. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, andkey skills; internal peer equity; as well as market and organizational considerations when extending an offer.

Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical anddental care programs, generous retirement benefits, and a wide array of family- friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/

Education

Completion of an Associate's degree

Experience

Work requires a minimum of two years of relevant research experience. Completion of the DOCR North Carolina state approved Clinical Research Apprenticeship program may substitute for one year of required experience. A Bachelor's degree may substitute for 2 years required experience.

Degrees, Licensures, Certifications

Work requires a minimum of two years of relevant research experience. Completion of the DOCR North Carolina state approved Clinical Research Apprenticeship program may substitute for one year of required experience. A Bachelor's degree may substitute for 2 years required experience.



Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy related conditions), sexual orientation or military status.



Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.


Essential Physical Job Functions:

Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and provision for requests for reasonable accommodation will be provided by each hiring department.


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CLINICAL RESEARCH COORDINATOR • Durham, NC, United States

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