Clinical Research Data Analyst

Public Trust: NACLC (T3)

Requisition Type: Regular

Your Impact

Own your opportunity to work alongside federal civilian agencies. Make an impact by providing services that help the government ensure the well being and support of U.S. citizens.

Job Description

GDIT's Military Health Team is hiring a Clinical Research Data Analyst to support the Traumatic Brain Injury Center of Excellence (TBI CoE) located at Ft. Bragg in Fayetteville, NC.

The Research Data Analyst will coordinate activities associated with clinical trials in the area of Traumatic Brain Injury (TBI) and provides assurance of accurate documentation in compliance with all governing regulations. They will serve as a liaison for collaborating between institutions, human subjects review boards, and commercial partners.

HOW A RESEARCH ANALYST WILL MAKE AN IMPACT:

• Runs basic statistical analyses using a standard statistical software package.
• Manages and analyzes data generated from large data sets, clinical investigational and research studies.
• Develop databases or modify existing databases to create datasets for analysis.
• Provides critical analysis of study results to assist in interpretation and decision making.
• Prepares documents reporting statistical analysis and descriptive data to be used in research reports.
• Assist in the development of reports or manuscripts.
• Prepares and/or presents research related manuscripts, scientific articles, posters, grant applications, and protocols with other investigators.
• Creates, maintains and updates various internal databases.
• Ensures data quality and statistic management of data, and appropriate handling and storage of data.
• Provides assurance of accurate documentation and maintain detailed account of any changes or updates in study protocol, data queries, etc.
• Coordinate with team regarding technical and/or clinical issues affecting research efforts.
• Coordinates and participates in activities associated with clinical trials in the area of TBI to include but not limited to protocol development, operational procedures and forms development, assistance in study implementation, data analysis, and technical reporting.
• Serves as a liaison for collaborating institutions, human subjects review boards, and commercial partners.
• Coordinates meetings as needed.
• Ability to obtain/ maintain a T3 security investigation.

WHAT YOU’LL NEED TO SUCCEED:

• Bachelor's Degree in public health-related field (BSPH) Statistics, or related field.
• 2+ years’ experience working with large clinical research datasets.
• Proficiency with statistical software (e.g., SAS, STATA) and social science research methodology.
• Excellent communication skills (both oral and written), basic clinical acumen, possesses writing and analytical skills and proficiency in research conduct are required.
• Excellent organizational skills necessary to keep track of updates/changes to protocol, etc.

GDIT IS YOUR PLACE:

• 401K with company match
• Comprehensive health and wellness packages
• Internal mobility team dedicated to helping you own your career.
• Professional growth opportunities including paid education and certifications.
• Cutting-edge technology you can learn from
• Rest and recharge with paid vacation and holidays

Work Requirements

Years of Experience

2 + years of related experience

* may vary based on technical training, certification(s), or degree

Certification

Travel Required

None