Research Assistant

Thank you for your interest in joining our team! This is an EVERGREEN job posting, meaning it is always open to qualified candidates, even if there isn’t an immediate opening. By applying, you’ll be added to our talent pool for this role or similar opportunities in the future. While we may not be actively hiring right now, we regularly review applications and keep your profile on file. If a suitable position becomes available, we’ll reach out to candidates whose skills and experience align with our needs. We encourage you to apply if you're interested in being considered for future opportunities with us. Even if we don’t have an opening at the moment, your application ensures we can connect with top talent like you when the right opportunity arises.

About The Position

The Research Assistant I provides assistance to the Principal Investigator and

Study Team coordinating research activities that may include recruiting participants, data collection and management and other research activities as assigned. The RA will assist with report generation and project close-out support.

This is an on-site position assigned to the Tripler Army Medical Center and Schofield Barracks in Hawaii. A thorough government background check will be required.

About The Project

This project aims to create a tool to improve decision-making on optimal return-to-duty (RTD) timing for service members following musculoskeletal (MSK) injuries. Key objectives include identifying treatment factors linked to successful RTD, assessing the prevalence of known risk factors across services, and tracking injury recurrence within six months post-RTD. The project also seeks to build adaptable prediction models that continuously integrate new data for improved RTD forecasting and to explore associations between RTD and long-term outcome. May assist in other projects as well.

Salary Range

$19.00 - $23.00/HOUR. Salaries are determined based on several factors including external market data, internal equity, and the candidate’s related knowledge, skills, and abilities for the position.

Qualifications

• Bachelor’s degree or equivalent work experience required
• 1 year experience in research preferred
• Non-profit, research, or healthcare experience desired
• Demonstrate competence in oral and written communication
• Must be organized, attentive to detail, and possess a positive, friendly and professional demeanor
• Must be flexible with changing priorities and able to communicate in a diplomatic and professional manner
• Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
• Familiarity with medical terminology, medications, laboratory tests, and abbreviations commonly used in patient medical charts
  
  
  

Responsibilities

• Adheres to Occupational Safety and Health Administration (OSHA), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), infection control procedures and rules and regulations pertaining to the research site
• Assist with self-reporting baseline assessment measures
• Assist with administrative logistics including consenting research participants, data collection, and scheduling
• Executes, maintains research study to include data collection
• Prepares research subjects (animal or human) for research study
• Manages study documentation to include accurate and timely filing
• Prepares progress reports
• Complies with all the rules and regulations as applicable to assigned duty station
• Documents all correspondence and communication pertinent to the research
• Interacts and communicates effectively with study and site personnel, research participants, The Geneva Foundation and the study sponsor
• Promotes safety and confidentiality of research participants at all times
• Creates and adheres to a data quality and quality assurance plan
• Assists with the initial coding and data entry of structured questionnaires and data collection tools, when applicable
• Demonstrates proficiency in performing basic study related procedures as required
• Maintains and updates files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.)
• Schedules and attends regular team meetings