Data Analyst

Georgetown University•Vinalhaven, ME

14d•$26 - $48•Onsite

About The Position

Georgetown University comprises two unique campuses in the nation’s capital. With the Hilltop Campus located in the heart of the historic Georgetown neighborhood, and the Capitol Campus, just minutes from the U.S. Capitol and U.S. Supreme Court, Georgetown University offers rigorous academic programs, a global perspective, and unparalleled opportunities to engage with Washington, D.C. Our community is a close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. Job Overview Data Analyst for Infectious Diseases Clinical Trials Unit will work with and assist the Clinical Research Coordinator, Regulatory Specialist, and Clinical Trial Manager by entering data into clinical trial sponsor system, as well as internal software. Work Interactions The Data Analyst will work with and assist the Clinical Research Coordinator, Regulatory Specialist, and Clinical Trial Manager by interacting with the clinical trial sponsor and also their propriety software for data entry. The Data Analyst may interact with clinical trial subjects to plan visits to the clinical trial, as well as schedule the subjects in Google Calendar. The Data Analyst will work with the Clinical Trial Coordinator and also Financial Administrator to ensure data between Georgetown GMS and clinical trial sponsor match. The Data Analyst will escalate necessary issues, such as data discrepancies, when discovered to the Clinical Trial Manager. Additional duties include, but are not limited to: Develops an understanding of research processes Documents business requirements of research processes Partners with clinical staff to help with the data requirements of research functions 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 Documents technical processes, as needed Verifies that recommended solutions align with research requirements 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 Assists with the testing and implementation of new system functionality 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

Requirements

3 years of experience working with clinical trials and supporting a clinical trial research staff, or a similar health care setting
Familiarity with Microsoft Word and Excel; Google Gmail, Calendar, and Drive required
Ability to communicate effectively
Capacity to interact with a diverse community
Ability to pay close attention to detail
Ability to work well under pressure
Ability to manage multiple tasks simultaneously
Ability to use independent judgement and discretion in determining the best course of action.
Ability to work with large data sets
Strong knowledge and familiarity of Microsoft Office applications
Ability to create and document procedures for training materials
Excellent problem-solving skills
Excellent communication skills
General knowledge of clinical research

Nice To Haves

Experience with Workday a plus

Responsibilities

Enter data into clinical trial sponsor system, as well as internal software.
Interact with the clinical trial sponsor and their proprietary software for data entry.
Plan visits to the clinical trial and schedule subjects in Google Calendar.
Ensure data between Georgetown GMS and clinical trial sponsor match.
Escalate necessary issues, such as data discrepancies, when discovered to the Clinical Trial Manager.
Develop an understanding of research processes.
Document business requirements of research processes.
Partner with clinical staff to help with the data requirements of research functions.
Create and document instructions for complex tasks so that others may use as a guideline in the future.
Test applications to confirm intended functionality, as well as identify gaps.
Assist with the creation of user training materials.
Document technical processes, as needed.
Verify that recommended solutions align with research requirements.
Develop understanding of software development lifecycle methodologies.
Effectively communicate with customers, internal resources and support teams to ensure objectives are met.
Collaborate with clinical and research resources to identify and develop process improvements.
Assist with the testing and implementation of new system functionality.
Participate in cross-functional teams to gather clinical and research needs in order to identify effective solutions.
Perform other projects and duties as assigned by the Clinical Research Manager.