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needed to gather data. Schedule and/ or call subjects for appointments. Order and maintain equipment and supplies. Process study compensation payments and thank you letters to subjects upon completion
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assigned. Additional Information Schedule: Full-time Job Code: 4751 Employee Status: Regular Grade: G Requisition ID: 103654 Work Arrangement : On Site
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renewals are completed. Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact
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for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact. Monitor expenditures and adherence to study
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contacting potential participants to schedule in-person study visits at a Stanford clinic; obtaining informed consent from participants for the research study; guiding participants through their study visits
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status, or any other characteristic protected by law. Additional Information Schedule: Full-time Job Code: 4121 Employee Status: Regular Grade: H Requisition ID: 106647 Work Arrangement : On Site
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, department manager, or chair in regards to establishing priorities and identifying and resolving problems that are administrative in nature. Oversee and/or perform duties associated with scheduling, organizing
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clinics, assisting with local presentations and outreach efforts, making phone contact with interested individuals, and scheduling laboratory visits. The CRCA will also be responsible for conducting formal
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responsibility. Responsible for hiring and retaining staff, career coaching, personal development for direct reports, and accountable for the performance of employees. Ensure work completion within the scheduled
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, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact. Monitor expenditures and adherence to study budgets and resolve