Job Summary
The Clinical Research Coordinator is responsible for overseeing oncology clinical trials, managing various study activities while prioritizing patient safety and adhering to protocol guidelines. This role involves facilitating patient recruitment, conducting screenings, and ensuring accurate data collection in collaboration with investigators and clinical team members.
Responsibilities
- Coordinate and manage oncology clinical trials
- Ensure compliance with research protocols and patient safety standards
- Assist in the recruitment and screening of trial participants
- Oversee data collection processes
- Collaborate closely with clinical staff and investigators
Qualifications
- Bachelor’s degree in a relevant field
- Minimum of 2 years of experience in clinical research, preferably in oncology
- Familiarity with EPIC EHR systems is an advantage
- Strong interpersonal and communication skills
- Proficiency in Microsoft Office applications
- Professional certification in clinical research is encouraged
