Clinical Research Analyst

Must be authorized to work in the United States

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 Clinical Research Analyst 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.

Job Description: 

The contractor shall:

• Work with Principal Investigators (PIs) on the development (e.g. study conceptualization, protocol development, selection of study procedures), implementation (e.g., subject coordination, data collection, database management, data analysis and interpretation of find-ings), and dissemination of research studies.

• Develop and maintain SPSS database for designated studies.

• Complete data management for enrolled subjects.

• Work with PIs to collaborate with other departments/ICs to design research projects.

• Provide administrative support for Principal Investigators.

• Provide manuscript development support and contribute with experience as author/co-author; write, edit and format manuscripts for publication.

• Develop and maintain reference database in End Note.

• Perform and organize library searches for the literature reviews; work with the team to develop and publish review papers.

Required Skills: 

The contractor must have:

• Bachelor’s degree in a related discipline.

• Minimum of two (2) years of experience in clinical research.

• Experience with clinical research protocols, including data entry and dissemination of findings.

• Experience with SPSS, End Note and Microsoft Office Suite.

• Strong communications skills, both oral and written.

• Excellent analytical, organizational and time management skills.