Clinical Research Study Coordinator

About this role

• Clinical Research Coordinator must have 1 or more years experience in clinical research and preferable experience in endocrinology or diabetes.
• The primary role is to coordinate phase II-IV clinical research for investigational new drug/device studies.
• Potential trials include Diabetes, Thyroid, Adrenal Hyperplasia, Parathyroid, Obesity and more.
• This is not a remote work position but some work may be done remotely.
• Responsibilities: Initiative recruitment and database searches for potential research candidates Involvement in patient screening and enrollment for the clinical studies Preparing and maintaining clinical trial source documents Conducting study visits, including vital signs, ECG, blood draw and processing Completing and ensuring the quality of case report forms Maintaining and dispensing drugs Preparing for site monitoring visits Preparing for site selection visits Maintaining documentation regarding all aspects of the study; Maintaining patient confidence and protects operations by keeping information confidential Maintaining and preparing site regulatory documentation for study start-up and during trial.
• Communicates with the IRB (site uses sponsor IRB) Skills/Qualifications: Must have 1 or more years of Research Coordinator experience Current IATA training certification preferred but can be completed upon hiring Current GCP certification preferred but can be completed upon hiring Required experience working with sponsors, IRBs and CROs Good interpersonal and organizational skills.
• Excellent computer and EMR skills.
• Demonstrate strong communication, leadership and presentation skills.
• Self-directed, proactive and timely in the management of the assignments.
• Job Type: Part-time Benefits: 401(k) 401(k) matching Health insurance Paid time off Monday to Friday Experience: Clinical Research/Clinical Trials: 1 year Pay: $20.00 - $40.00 per hour Benefits: * 401(k) * Flexible schedule * Health insurance * Paid time off Experience: * Clinical trials: 1 year (Required) * Clinical research: 1 year (Required) * GCP: 1 year (Required) * Research: 1 year (Required) Work Location: In person

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