Study Manager

• Ensure that all outside vendor contracts are set up and deliverables are being meet in accordance to the agreed upon work order.
• Obtain and review clinical statement of work (SOW) and/or study work order (SWO) to determine what services are required for each clinical trial protocol.
• Initiate and participate in the early planning phases of clinical study by providing guidance on deliverables and outsource options (i.e. assist in preparation of study proposal timelines, scheduling and other study requirements as appropriate); including but not limited to study source documents, procedural timelines and lab set up.
• Work closely with clinical research coordinator to ensure adequate internal resources and resolution of any clinical study work flow issues for assigned clinical studies.
• Prepare and maintain project management plan for assigned clinical studies.
• Act as liaison and point of contact for all clinical study sponsors and vendors for related services.
• Attend sponsor meetings and required conference calls to ensure effective communication flow between external customers and staff.
• Present at Clinical Tracking Meetings

ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment