Clinical Research Coordinator

Responsibilities

• Work with the Principal Investigators, treating physicians, and research nurse to confirm that each patient meets eligibility criteria specified by protocols for enrollment into clinical trials.
• Manage study recruitment activities in person and over the phone.
• Conduct protocol-specific consenting process.
• Collect, process, store, and ship participants’ specimens as per protocol.
• Prepare for and conduct study visits, including family counseling activities.
• Enter and maintain research data, ensuring data quality, integrity, and compliance with all regulatory, institutional, and departmental requirements.
• Responsible for accountability of clinic and office supplies.
• Presents and implements adapted onboarding plans with activities, goals, and time plans.
• Participate in community outreach activities as a liaison.
• Complete required regulatory tasks, including IRB submissions, protocol/consent form modifications, maintenance of regulatory binders, and preparation for site visits.
• Uses Quality Improvement Standards and practices to influence care teams to adopt best practices.
• Perform related duties & responsibilities as assigned/requested by PI, study clinicians and/or study manager.

Qualifications

• Bachelor's degree or equivalent in education and experience required.
• Bilingual in English and Spanish preferred.