Research Outcomes Data Coordinator

Sentara Health’s Clinical Trials Office located at Sentara Norfolk General Hospital is hiring a Research Outcomes Data Coordinator!

This position is full time day shift working 8am to 5pm Monday through Friday.

Sentara Health Research Center provides scientific, administrative, and regulatory support for research conducted across Sentara Healthcare and in our communities.

Sentara Health Research Center strives to improve treatment options, medical technology, and health equities with our dedicated team of experts and state-of-the-art technology.

Our Clinical Trials are conducted in the hospital and medical practice settings.   We also conduct research in our community with our many community practices. Our research helps to advance scientific understanding of diseases and advance knowledge that leads to better and more effective treatments that improve the health in our communities.

Responsibilities:

Serves as the liaison between the Sentara Health Research Center and investigators (physicians, students’ residents, etc) to provide project management for research study requests.  Collaborates with investigators, regulatory specialists, system data analytics and other research specialists to complete projects timely.

Will work closely with the clinical researcher to assist with project development, cohort definition, data collection, tool development, IRB proposal, Sentara Portal submissions, and other project tasks as assigned.

Demonstrates strong knowledge of regulatory guidelines (ICH-GCP, FDA, etc.) to ensures all study projects meet and are maintained per the regulatory and compliance guidelines.

Facilitates discussions and assists in preparing protocol development ensuring source and methods of data collection are within regulatory and Sentara guidelines. 

Works collaboratively with System Data Analytics to ensure timely data curation and analytical support and helps to determine need and resource for any additional necessary statistical support.

Assists with aspects of manuscript preparation and submission such as preparing data tables and figures, formatting references, etc.

Maintains awareness of grant opportunities and works closely with researchers on completing grant submissions.

Proficient with MS Office and experience working with clinical data management tools and processes. 

Experience/Education:

Master’s Level Degree required.  (Examples: Master of Public Health or Epidemiology)

2 years of related research or healthcare work experience

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• ACRP
• SOCRA

• Master's Level Degree
• Master's Level Degree

• Related 2 years