Clinical Research Coordinator

Employment Type: 6-month contract to hire

Schedule: 8:00am-5:00pm (may require flexibility based on patient visits)

Need at least 2 years of prior CRC experience

• Assist with the design, coordination, and execution of research projects under the guidance of senior researchers.
• Collect, organize, and manage quantitative and qualitative data from clinical, survey, and digital health sources.
• Conduct literature reviews and summarize findings to support study development and publication efforts.
• Ensure compliance with research protocols, ethical standards, and data privacy regulations (e.g., HIPAA).
• Prepare research materials, consent forms, and documentation for IRB submissions.
• Support the preparation of reports, presentations, and manuscripts for internal and external use.
• Collaborate with interdisciplinary teams, including clinicians, data scientists, and policy experts.
• Maintain accurate project records and track study milestones and deliverables.
• Occasional travel may be required for audits, site visits, or team meetings (confirmed talent will not be driving while on the clock).

• Strong organizational and time-management skills
• Proficiency in Microsoft Office Suite and basic data management tools (e.g., Excel, REDCap, Qualtrics)
• Excellent written and verbal communication skills
• Detail-oriented, proactive, and able to work independently and collaboratively

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