Shire Jobs

This job was posted by https://www.kansasworks.com : For more information, please see: https://www.kansasworks.com/jobs/12897415

Key Responsibilities:

• Extrapolate data from source records into case report forms for all patient visits.
• Ensure timely data submission in accordance with USOR SOPs.
• Responsible for resolving queries, communicating concerns or questions about data to clinical staff and or research management.
• Utilizes USOR clinical trial management system to access research forms and keep current all applicable patient reporting and tracking functions, including but not limited to subject CRF binders/folders.
• May be responsible for coordinating patient billing and research payout/payment tracking.
• Maintains research records in a confidential manner according to practice policies, sponsor confidentiality agreements, HIPAA guidelines and any other applicable regulations.
• Coordinates monitoring and auditing visits ensuring that all data and queries are entered and resolved in accordance with the USOR and sponsor requirements.
• Assists with investigational drug accountability process, ordering and maintaining research supplies.
• Schedules patients follow up appointments and/or procedures required to maintain protocol compliance.
• Collecting and processing of specimens, imaging documents and other items required for research purposes.
• Acts as resource for other for training and education of other data coordinators at the site/location.