Clinical research coordinator vs clinical research specialist

Differences between clinical research coordinator and clinical research specialist duties and responsibilities

Clinical research coordinator example responsibilities.

• Assess study participants for adverse reactions or complications and manage side effects of chemotherapy and other study relate drugs.
• Establish and maintain strong community partnerships to achieve HIV prevention objectives.
• Direct acquisition and analysis of functional MRI research data following GCP and FDA regulations
• Prepare and maintain IRB and regulatory documentation for various research projects and consent patients for clinical research.
• Facilitate constant communication between principal investigators, oncology nurses, and patients to address concerns and maximize eligibility and enrollment.
• Schedule patient for study procedures; initiate/coordinate drug orders, laboratory procedures and treatments for patients base on standing protocol orders.
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Clinical research specialist example responsibilities.

• Manage the input of the subjects' data among various management database including iMedidata, EDC.
• Develop and project manage a staffing program model to support inpatient oncology.
• Manage all planning and execution of oncology clinical trials, domestic and international, including decision impact and companion diagnostic trials.
• Review and edit clinical documentation for FDA submission and approval.
• Prepare investigator initiate and industry study protocol for IRB review and approval.
• Participate in study developments to ensure compliance with FDA regulations and guidelines.
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