Roles and responsibilities
Must be authorized to work in the United States
W2 with full benefits
Some travel may be required
Offer contingent on ability to successfully pass a background check and drug screen
Columbus Technologies and Services Inc. is a strategic supplier and business partner to the federal government and its key suppliers. Through our partnership with the National Institutes of Health, Columbus offers administrative, IT, engineering, scientific, and healthcare professionals the opportunity to work with one of the most prestigious research organizations in the world. We are currently seeking a Clinical Protocol Coordinator to work onsite with the National Institutes of Health in Bethesda, MD.
This is a long-term position which offers:
- Competitive salary
- Tremendous growth opportunity
- Opportunity to work at NIH, the world's foremost medical research center
- Learn more about what Columbus can do for you at www.columbususa.com
• Coordinate development of study activities for Connect, such as developing protocols and IRB documents for tissue and image collection at partnering health care systems, with the study management team, scientific investigators, and partnering health care system study teams.
• Coordinate development of a rapid case ascertainment together with the study management team, scientific investigators, and partnering health care system study teams.
• Research evidence and best practices to integrate into the development of study activity and rapid case ascertainment protocols.
• Coordinate development of related dashboard modules, including testing of IT infrastructure.
• Assist on all aspects of epidemiologic cancer research, including data management (data coding and cleaning, specimen tracking), analysis (entry level statistical analysis of epide-miologic and laboratory data), and preparation of reports for presentation or publication
• Coordinate and maintain communications by organizing meetings and teleconferences, agendas and meeting notes, actions items and decision logs, and tracking and responding to issues requiring resolution.
• Support with internal information flow within the Division on the study progress, such as updating the Division intranet site and responding to inquiries from investigators.
• Prepare presentations, reports, and manuscript writing as needed.
• Assist with compiling data needed for budget planning.
• Required: MPH/MA/MS and at least two years of research experience
• Preferred: Experience in government or academic health research
• Must demonstrate a history of proven success in study management and/or statistical analyses
• Highly detail oriented
• Excellent communication skills (email, written, and verbal)
• Work with a multi disciplinary team with varying skill levels and to liaise with multiple stakeholders
• Able to work on multiple tasks simultaneously and effectively prioritize work in a fast paced environment
• Work independently and seek guidance appropriately
• Ability to assist with both routine and/or last minute projects
• Advanced skills in Microsoft Office software and familiarity with citation management programs