Georgetown University's Infectious Diseases Clinical Trials Unit needs a Part Time Data Analyst to assist with data entry, documentation, and process improvement for clinical trials.
Requirements
- Familiarity with Microsoft Word and Excel; Google Gmail, Calendar, and Drive required
- Ability to work with large data sets
- Strong knowledge and familiarity of Microsoft Office applications
- Ability to create and document procedures for training materials
- Experience with Workday a plus.
Responsibilities
- entering data into clinical trial sponsor system, as well as internal software.
- Documents business requirements of research processes
- Creates and documents instructions for complex tasks so that others may use as a guideline in the future
- Tests applications to confirm intended functionality, as well as identify gaps
- Assists with the creation of user training materials
- Verifies that recommended solutions align with research requirements
- Assists with the testing and implementation of new system functionality
Other
- Develops an understanding of research processes
- Partners with clinical staff to help with the data requirements of research functions
- Develops understanding of software development lifecycle methodologies
- Effectively communicates with customers, internal resources and support teams to ensure objectives are met
- Collaborates with clinical and research resources to identify and develop process improvements
- Participates in cross functional teams to gather clinical and research needs in order to identify effective solutions
- Performs other projects and duties as assigned by the Clinical Research Manager
- Must possess the ability to communicate effectively and have the capacity to interact with a diverse community and use independent judgement and discretion in determining the best course of action
- pay close attention to detail, work well under pressure and manage multiple tasks simultaneously,
- Excellent problem-solving skills
- Excellent communication skills
- 7 years of experience working with clinical trials and supporting a clinical trial research staff, or a similar health care setting
- 5 years of experience working with clinical trials and supporting a 5 year clinical trial research staff, or a similar health care setting
