Clinical research monitor vs senior program coordinator

Differences between clinical research monitor and senior program coordinator duties and responsibilities

Clinical research monitor example responsibilities.

• Manage a consultant to review scientific support and create dossiers on each product that make health claims in the EU.
• Maintain CTMS project tracking system of subject and site information and essential documents.
• Collect and review all initial regulatory documents from site for submission to IRB and sponsor.
• Coordinate and conduct the training of site personnel on protocols, CRF review and conduct source document verification.
• Resolve CRF discrepancies and/or clarifications via site visit, telephone, email or fax as deemed appropriate for the study.
• Prepare high quality site documents and collect country-specific information for IRB processes.
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Senior program coordinator example responsibilities.

• Manage co-op vendor and provide overall program direction for Toyota dealers and regional offices nationwide.
• Report metrics associate with assign compounds to QA management, clinical development clinical development staff, and contract research organization staff.
• Participate at PPT's and participate in the development of IEP's and strategies to meet IEP objectives.
• Coordinate RFP policies and processes for all grant programs to ensure consistency.
• Collaborate with home inspector to create scope of work, prepare RFP s to secure construction bid quotes from rehabilitation contractors.
• Schedule and facilitate all IEP meetings, gathering information, inviting participants and encouraging parent participation.
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