Clinical Research Coordinator (CRC/CRN) - 256393

Key Responsibilities


- Lead the execution of clinical trial protocols, maintaining strict protocol adherence, safety standards, and study timelines.
- Coordinate patient care, schedule trial activities, conduct consenting, and manage patient visits.
- Complete safety and Adverse Event (AE) data entry, manage electronic data capture (EDC) entries, and resolve queries.
- Maintain accurate trial notes, regulatory documentation, and compliance records.
- Manage a structured workload averaging 5–7 complex patient visits per week (capped at a maximum of 3 visits per day).
- Participate in cross-coverage within disease pods to ensure seamless support across the study portfolio.


Work Hours & Schedule


- First 90 Days: Standard 8-hour schedule during onboarding and preceptor training (typically 8:00 AM – 4:00 PM or 9:00 AM – 5:00 PM).
- Post-90 Days: Flexible 8-hour daily schedule with customizable start times between 6:30 AM and 9:00 AM.


Requirements


- Non-RN Candidates: Minimum 3+ years of dedicated clinical research experience (5+ years preferred).
- RN Candidates: Minimum 3+ years of clinical nursing experience required (oncology experience preferred).
- Experience with clinical trial execution, regulatory standards, EDC platforms, and query management.
- Prior experience in oncology, investigational drug trials, or complex Phase I–III protocols is strongly preferred.
- Exceptional organization, task management, and communication skills.