This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
The clinical research assistant will be an integral member of Dr. Eseosa Ighodaro’s clinical research team, dedicated to advancing stroke care through innovative interventions and quality improvement initiatives. Working under the direct supervision of Dr. Ighodaro, this role involves performing a broad range of technical and administrative responsibilities to support research activities within clinical settings. US citizens or permanent residents only. The incumbent will contribute to the success of studies aimed at improving stroke care for patients at Atrium Health Wake Forest Baptist Hospital, ensuring accuracy, compliance, and operational efficiency throughout all phases of research. Key responsibilities include assisting with data collection and analysis, coordinating study logistics, maintaining regulatory documentation, and supporting scholarly outputs such as manuscripts and presentations. This position requires exceptional organizational skills, meticulous attention to detail, and the ability to work independently while thriving in a collaborative, multidisciplinary environment. The role is contingent upon grant funding and offers an opportunity to make a meaningful impact on patient outcomes and the community.
Job Responsibility:
Assist in developing research methodologies and protocols
Create and revise study materials
Conduct participant recruitment, screening, and interviewing, and follow-up activities for research studies
Perform data collection and analysis
Generate study reports
Conduct literature reviews to support ongoing studies
Prepare tables, figures, and data reports for manuscripts and grants
Assist in writing research content for publications and presentations
Format and submit papers to journals
Submit IRB applications for research and quality improvement studies
Maintain regulatory documentation
Ensure all aspects of the study comply with protocol and institutional standards
Attend research meetings and take detailed notes
Schedule research meetings
Order supplies for research projects
Help train new personnel (undergraduates, medical students, resident physicians, fellow physicians)
Serve as a liaison between the study team and research participants or community members
Requirements:
Master's degree with four years' experience in a research setting
or, an equivalent combination of education and experience
Clinical experience preferred
Understanding of scientific research methodologies
Ability to prepare grant proposals independently
Experience with peer-reviewed publications and poster/oral presentations
Proficiency in Microsoft Word, Excel, PowerPoint, and basic statistical analyses
Ability to manage and analyze data accurately
Strong written and verbal communication
Detail-oriented, resourceful, and able to meet deadlines consistently
Works well in multidisciplinary teams and contributes effectively to group projects
Ability to troubleshoot research challenges and adapt to evolving study needs
Self-starter capable of working with minimal supervision
Maintains a professional appearance and demeanor
relates well to all organizational levels
US citizens or permanent residents only
What we offer:
Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs
Educational Assistance Program
Opportunity for annual increases based on performance
Premium pay such as shift, on call, and more based on a teammate's job