Part Time Clinical Research Coordinator

Benefits

Qualifications

• •The ideal candidate has hands-on clinical research experience, strong organizational skills, and the ability to engage confidently with participants and research staff
• •Previous experience as a Clinical Research Coordinator is required
• •Bilingual (English/Spanish) required
• •Oncology clinical trial experience required
• •Experience with electronic medical records (EMR) and electronic data capture (EDC) systems
• •Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members
• •Demonstrated accuracy in documentation, data entry, and protocol adherence
• •Maintaining an inclusive environment through persistent self-reflection
• •5 more items(s)

Responsibilities

• •Contract Duration: Open-ended (estimated 3–6 months)
• •Schedule: 10-20 hours per week, Monday–Friday during standard business hours
• •We are seeking a detail‑oriented and proactive Clinical Research Coordinator (CRC) to support an ongoing Oncology clinical trial
• •This contractor will function as one of the primary CRCs for the study and must be able to work independently while managing multiple study activities
• •Identify, recruit, and prescreen potential participants for eligibility
• •Conduct phone screenings and review inclusion/exclusion criteria
• •Perform thorough reviews of patient medical records to determine suitability
• •Data & Documentation Management
• •Collect and enter study data into electronic data capture (EDC) systems with a high degree of accuracy
• •Resolve EDC data queries promptly
• •Retrieve necessary medical records and ensure proper documentation
• •Building a culture of care, engagement, and recognition with clear outcomes
• •9 more items(s)