1

Redcap Data Manager Jobs in Washington (NOW HIRING)

... REDCap. * Excellent interpersonal skills for conducting interviews and follow-up calls. Skills * Clinical Trial Administration * Regulatory & IRB Compliance * Participant Management * Data Security ...

Solutions Architect (Public Trust)

Reston, VA ยท On-site

$65.50 - $86.25/hr

Join our community of management consultants, mission-driven technologists, data scientists ... Experience working with data collection platforms like Qualtrics, REDCap, Microsoft Forms

Showing results 21-37

Redcap Data Manager information

What is a Redcap data manager?

Redcap Data Managers are professionals responsible for designing, implementing, and maintaining databases using the REDCap (Research Electronic Data Capture) platform. They ensure data integrity, manage user access, provide technical support, and oversee data collection processes in research studies or clinical trials. Their role often includes training research staff, troubleshooting issues, and ensuring compliance with data security and regulatory standards. Redcap Data Managers play a vital part in facilitating accurate and efficient data management for research projects.

What are the key skills and qualifications needed to thrive as a Redcap data manager, and why are they important?

To thrive as a Redcap Data Manager, you need expertise in data management, database design, and an understanding of research protocols, often supported by a degree in health informatics, information science, or a related field. Proficiency with the REDCap platform, knowledge of data security practices, and sometimes familiarity with statistical software or programming languages like SQL are typically required. Strong attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies ensure accurate data collection, compliance with research standards, and seamless collaboration with research teams.

How does a Redcap data manager collaborate with research teams to ensure data quality and compliance?

A Redcap Data Manager works closely with principal investigators, research coordinators, and IT staff to design, implement, and maintain data collection instruments within the REDCap system. They regularly communicate with team members to provide training, troubleshoot issues, and ensure proper data entry protocols are followed. Additionally, they play a vital role in monitoring data for accuracy, managing user permissions, and ensuring compliance with institutional and regulatory standards such as HIPAA. This collaborative environment helps foster reliable data collection and supports successful research outcomes.
What cities in Washington are hiring for Redcap Data Manager jobs? Cities in Washington with the most Redcap Data Manager job openings:

Scientific Program Analyst

N4 Solutions, LLC

Bethesda, MD

Full-time

Posted 24 days ago


Job description

JOB DESCRIPTION/DUTIES:

The Scientific Program Analyst will support the National Institutes of Health (NIH), Clinical Center (CC), Department of Bioethics by providing scientific research, program coordination, manuscript management, and data analysis support for ongoing clinical and bioethics research initiatives. The successful candidate will collaborate with multidisciplinary research teams to support research studies, scientific publications, departmental educational programs, and research operations while ensuring the efficient coordination of multiple concurrent projects. This description reflects the current responsibilities performed in the role in addition to the foundational data management responsibilities identified in the Task Order.

· Conduct comprehensive literature reviews to support clinical and bioethics research projects.

· Assist investigators with qualitative and quantitative research studies.

· Conduct participant interviews and support qualitative data collection efforts.

· Perform qualitative coding and thematic analysis using qualitative research software.

· Conduct basic statistical analyses and prepare data summaries to support research initiatives.

· Create publication-quality tables, graphs, figures, and visualizations for scientific manuscripts and presentations.

· Edit, format, and coordinate scientific manuscripts for internal NIH review and submission to peer-reviewed journals.

· Maintain departmental manuscript tracking databases and publication records.

· Coordinate internal manuscript review workflows and monitor publication status.

· Organize and maintain research documentation, shared files, and departmental databases.

· Coordinate departmental educational programs, seminars, and scientific meetings.

· Schedule meetings, communicate with faculty and guest speakers, prepare agendas, and distribute meeting materials.

· Coordinate speaker logistics, reimbursements, certificates, and audiovisual support for departmental educational events.

· Serve as the primary coordinator for Research Methods Series meetings, Empirical Research Lab meetings, and other departmental scientific activities.

· Record meeting minutes, document action items, and maintain meeting records.

· Coordinate Clinical Center Ethics Committee meetings and prepare meeting documentation.

· Research, evaluate, and assist with implementation of software platforms and research management systems.

· Develop and improve research tracking tools and workflow processes to increase operational efficiency.

· Perform data validation, quality assurance (QA), and quality control (QC) activities to ensure research data integrity.

· Develop and maintain research databases, tracking spreadsheets, and documentation.

· Utilize Microsoft Excel and automation techniques to organize, reconcile, and validate large research datasets.

· Collaborate with investigators, clinicians, statisticians, and research staff across multidisciplinary teams.

· Maintain confidentiality of research data and comply with NIH policies and research regulations.

· Prepare reports, presentations, and other scientific documentation.

· Perform other duties as assigned.

EDUCATION / EXPERIENCE / EXPERTISE REQUIREMENTS:

· Bachelor's degree in Public Health, Bioethics, Biology, Psychology, Neuroscience, Biomedical Sciences, Statistics, Sociology, Philosophy, Health Sciences, or a related scientific discipline.

· Minimum one (1) year of experience supporting clinical, biomedical, academic, or public health research.

· Experience conducting literature reviews and scientific research.

· Experience supporting scientific manuscripts, publications, or technical writing.

· Experience coordinating research projects or scientific programs.

· Experience organizing meetings, educational events, or research initiatives.

· Strong organizational and project management skills with the ability to manage multiple priorities.

· Excellent written and verbal communication skills.

· Strong analytical, critical thinking, and problem-solving abilities.

· Experience with Microsoft Office Suite, including Excel, Word, PowerPoint, Outlook, and Teams.

· Ability to work independently while collaborating effectively within multidisciplinary teams.

PREFERRED EDUCATION / EXPERIENCE / EXPERTISE:

· Master's degree in Public Health (MPH), Bioethics, Psychology, Statistics, Data Science, Epidemiology, Health Sciences, or a related field.

· Experience supporting NIH, HHS, academic medical centers, or biomedical research organizations.

· Experience with qualitative research methodologies.

· Experience using NVivo, Covidence, R, Qualtrics, REDCap, or similar research software.

· Experience performing qualitative coding or statistical analyses.

· Experience coordinating scientific meetings or educational programs.

· Experience preparing figures, tables, and visualizations for publications.

· Experience supporting systematic reviews or evidence synthesis projects.

· Knowledge of research compliance, manuscript review processes, and scientific publishing.

· Experience working in clinical research, bioethics, or public health research environments.

LOCATION:

· Bethesda, MD

· Full-Time (40 hours per week)

· On-site / Telework Eligible (per NIH policy)