
Clinical Study Coordinator
2 weeks ago
Study Coordinator Position
We are seeking a highly organized and proactive individual to support the daily operations of our longitudinal clinical trials. The study involves continuous glucose monitoring, lab testing, gut microbiome analysis, and remote consultations with physicians.
Main Responsibilities:
- Scheduling and follow-up on appointments for CGM setup, lab tests, stool sample collection, and virtual consultations.
- Data collection and management: monitoring and collecting data from wearable CGM devices and study-related apps, ensuring timely entry and validation of participant data in study databases or CRFs (Case Report Forms).
- Liaison between participants, clinical labs, logistics partners, and physicians, maintaining regular communication with participants to encourage adherence and resolve concerns.
- Maintaining accurate participant records in accordance with GCP and IRB protocols.
The ideal candidate will play a critical role in coordinating participant involvement, ensuring accurate data collection, and maintaining clear communication among all stakeholders. Key qualifications include a Bachelor's degree in a health-related field, experience in clinical research or healthcare setting, knowledge of lab logistics and biospecimen handling, and proficiency in using spreadsheets, EDC platforms, or research data systems.
Key Qualifications:
- Bachelor's degree in a health-related field.
- Experience in clinical research or healthcare setting.
- Knowledge of lab logistics and biospecimen handling.
- Proficiency in using spreadsheets, EDC platforms, or research data systems.
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