Company Description
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Role Description
This is a part time on-site role for a Clinical Research Coordinator located in Dartmouth, MA. The Clinical Research Coordinator will be responsible for managing day-to-day activities of clinical research trials. This includes obtaining informed consent from study participants, ensuring adherence to protocols, and maintaining accurate and detailed records. The role also involves coordinating with medical staff, sponsors, and regulatory bodies to ensure the successful implementation and execution of clinical trials.
Qualifications
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