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• Develops understanding of software development lifecycle methodologies • Effectively communicates with customers, internal resources and support teams to ensure objectives are met • Collaborates with
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will manage regulatory matters for complex clinical trials across multiple studies and therapeutic areas. The CTTM supports research efforts for various clinical trials within CTTM and Department
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business units to exchange and share data records, sometimes navigating multiple and incongruent data sources and storage methods, which requires an integrative mindset. Contribute to effective data
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for managing registration and attendance tracking for Advancement events which support the alumni engagement, development, and campaign goals established by the university. Additional duties include, but are not
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to communicate effectively; ability to work under pressure and respond to multiple demands; and must be sensitive to confidential nature of the job. Requirements and Qualifications Knowledge of professional
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multiple objects using out of the box and packaged data loading tools. Experience developing and implementing user types, profiles, record types, and custom security configuration. Ability to write basic
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University Medical Center (GUMC). Working under the direct supervision of the Director of the CRO, the CRC will manage regulatory for complex clinical trials across multiple studies and therapeutic areas
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development in the world of program management. Key responsibilities include extensive client interaction and communication, in person and virtually, on a daily basis across cultures and borders to support the
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University Hospital HD Center of Excellence. You will be part of our growing Huntington’s Disease Society of America (HDSA) Center of Excellence Interdisciplinary Team facilitating the development and
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sound judgment and knows when to escalate issues and when to manage independently. Exceptionally organized, detail-oriented, and able to manage multiple tasks while meeting deadlines. High level of