73 evolution "https:" "https:" "https:" "Multiple" positions at Georgetown University
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the MBA Program Associate Dean and Assistant Dean and manage one other professional staff member in order to guide strategy, programmatic development, and operations in the MBA Program Office. The Director
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multiple compliance tasks and deadlines. Attention to detail, especially for record‑keeping, certifications, and safety documentation. Good communication skills, both written and verbal; ability to interact
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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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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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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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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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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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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 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