Research Scientist (Contractor)

About Us

We are a nonprofit organization committed to supporting research and enhancing care and outcomes for individuals with type 1 diabetes. Our mission is to help people living with type 1 diabetes experience better, longer lives.

Role Overview

This temporary contract role offers research support to the Real-World Evidence (RWE) and Research team, addressing project needs as they arise. The Research team engages in observational, qualitative, and mixed-methods research to improve outcomes for people with type 1 diabetes, utilizing real-world data from the T1D Exchange Quality Improvement Collaborative and Registry. The current short-term need spans from October 2026 to January 2027, with additional opportunities possible.

Key Responsibilities

• Design and carry out research projects from initial hypothesis through dissemination using qualitative, quantitative, and mixed-method approaches.
• Conduct literature reviews and consult with sponsors/stakeholders to guide study design and objectives.
• Create study materials such as protocols, consent forms, surveys, and data collection instruments.
• Collaborate with internal teams and external partners to implement observational studies using real-world data and survey methods.
• Manage recruitment, data collection (qualitative and quantitative), data handling, and study monitoring when relevant.
• Perform or assist with data analysis and interpret research outcomes.
• Prepare and deliver research plans, progress summaries, and findings presentations to various audiences.
• Draft, revise, and contribute to scientific documents including abstracts, posters, manuscripts, and reports suitable for publication.
• Build and sustain partnerships with investigators, sponsors, and research collaborators.
• Stay informed on best practices in observational and patient-focused research, Good Clinical Practice, and compliance with applicable laws and regulations.
• Undertake other research-related responsibilities as needed.

Qualifications

• Master's degree or higher in public health, epidemiology, health services research, psychology, sociology, or related health/social science.
• At least two years of experience in conducting observational, qualitative, quantitative, or mixed-methods research.
• Proficient in developing and implementing research including literature reviews, protocol development, consent processes, survey creation, data analysis, interpretation, and dissemination.
• Familiarity with human subjects regulations and IRB procedures.
• Strong skills in scientific writing, communication, and presenting research findings.
• Excellent organizational, project management, and problem-solving abilities with meticulous attention to detail.
• Capable of working independently and collaboratively with diverse stakeholders.
• Preferred experience includes working with research sponsors, healthcare entities, or pharmaceutical industry.
• Experience specific to diabetes research and patient-reported outcomes is desirable.

Compensation

The position offers an hourly rate ranging from $70 to $90, dependent on candidate experience.