Clinical Research Assistant

Overview

We are seeking a motivated Research Assistant to support the planning, coordination, and execution of healthcare research initiatives. This role works closely with senior researchers and interdisciplinary teams to ensure high-quality study implementation, data integrity, and regulatory compliance.

• Support the design, coordination, and day-to-day execution of research studies under the guidance of senior investigators.
• Collect, organize, and manage quantitative and qualitative data from clinical settings, surveys, and digital health platforms.
• Conduct comprehensive literature reviews and synthesize findings to inform study design, analysis, and publication efforts.
• Ensure adherence to research protocols, ethical guidelines, and data privacy regulations, including HIPAA.
• Prepare study materials, informed consent documents, and supporting materials for Institutional Review Board (IRB) submissions.
• Assist in the development of reports, presentations, and manuscripts for internal stakeholders and external audiences.
• Collaborate with cross-functional teams, including clinicians, data scientists, and policy experts.
• Maintain accurate study documentation and support tracking of project timelines, milestones, and deliverables.

• Opportunity to contribute to meaningful healthcare research that advances innovation and health equity.
• Ongoing mentorship and professional development in research methodologies and health analytics.
• A collaborative, mission-driven team environment.
• Competitive compensation and comprehensive benefits package.

Required:

• Phlebotomy experience.
• Strong organizational and time-management skills with the ability to manage multiple priorities.
• Proficiency in Microsoft Office Suite and familiarity with data management tools such as Excel, REDCap, or Qualtrics.
• Excellent written and verbal communication skills.
• Highly detail-oriented, proactive, and capable of working both independently and as part of a team.

Preferred:

• Prior experience in clinical, epidemiological, or behavioral health research.
• Familiarity with research ethics, IRB processes, and data protection standards.