Clinical Research Coordinator

Our Clinical Research Coordinator will plan, direct, and coordinate Clinical Research studies in conjunction with the Medical Physician.

Schedule

• Monday through Friday

What You'll Do:

• Participates in the design of clinical studies, ensuring meaningful endpoints are captured for analysis
• Contacts potential study participants, obtain agreements, and study director approvals
• Collects appropriate medical history to ensure study participant eligibility.
• Reviews study objectives and study participant restrictions or limitations for the study
• Collects data obtained from research in a systematic and organized manner.
• Monitors the study to ensure that it complies with protocols, is ethically conducted, and follows regulatory standards
• Maintains research records of study activity, including case report forms, treatment records, or other regulatory forms as per FDA guidelines
• Makes sure that all equipment and supplies needed for the study are in-stock and in good working order
• Takes lead in monitoring IRB submission and review

Skills and Experience:

• Previous experience as a Clinical Research Coordinator is required
• Knowledge of Clinical Research regulations and GCP guidelines
• Strong organizational and time management skills
• Excellent interpersonal and communication skills

In support of our mission statement, "Healthier Practices, Healthier Patients", we have adopted a tobacco-free environment and we choose not to hire tobacco and nicotine users, including the use of e-cigarettes/vaping.