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Job Description
We areseekinga highly organized and proactivePatient Co-ordinator& Clinical Research Associate to support the daily operations of our longitudinal clinical trials. The study involves Continuous Glucose Monitoring (CGM), lab testing, gut microbiome analysis, and remote consultations with physicians. The ideal candidate will play a critical role in coordinating participant involvement, ensuringaccuratedata collection, andmaintainingclear communication among all stakeholders including patients, labs, physicians, and the internal research team.
Key Responsibilities
Participant Coordination:
Schedule and follow up on appointments for CGM setup, lab tests, stool sample collection, and virtual consultations.
Provide clear instructions and support to participants for app usage and test procedures.
Data Collection & Management:
Monitor and collect data from wearable CGM devices and study-related apps.
Ensuretimelyentry and validation of participant data in study databases or CRFs (Case Report Forms).
Flag and report data inconsistencies or protocol deviations to the study coordinator or PI.
Communication & Support:
Act as a liaison between participants, clinical labs,logisticspartners, and physicians.
Maintainregular, empathetic communication with participants to encourage adherence and resolve concerns.
Coordinate specimen shipment and tracking with third-party labs.
Documentation & Compliance:
Maintainparticipant data such as participant information sheets, consentforms.
Required Skills & Qualifications:
Job ID: 145396261