Registered Nurse – Clinical Research Coordinator – Oncology

• Evaluates, initiates, and maintains all activities related to the conduct of clinical trials in assigned area(s) of responsibility
• Communicates with external funding agencies, sponsors, departments, and patients to ensure understanding of the requirements of conducting and participating in clinical trials
• Organizes and manages all patient care requirements
• Provides patient care and assessment as determined necessary by the clinical trial in coordination with other care providers
• Participates in clinical trial selection with research leadership and organizes strategies for recruiting study participants and screening study participants for eligibility on the telephone, in the clinic, and other settings as required
• Uses the nursing process to ensure protocol compliance including patient recruitment, engaging in informed consent, patient education, and oversight of investigational drug administration schedule
• Coordinates and oversees patient activity as it relates to the conduct of research and clinical trials, monitoring patients for safety and adverse events during medical procedures
• Completes and/or supervises staff for the completion of case report forms on assigned protocols within the timeframe required by the study

• Associate degree in nursing
• 3 years of experience in area of assigned clinical specialty including 2 years performing clinical research, or 2 years of relevant research experience in a clinical setting
• Current registered nurse license in state of practice
• Basic Life Support (BLS) from the American Heart Association
• Working knowledge of ICH guidelines for ethical conduct of research
• Strong problem solving and critical thinking skills
• Ability to follow and provide critical feedback on the investigational plan
• Ability to train junior staff members in standard operating procedures and other related research activities

Demonstrates expertise in conducting clinical trials, including patient recruitment, protocol compliance, and oversight of investigational drug administration. Proficient in collaborating with research leadership and external stakeholders to ensure successful trial execution and patient safety.

• Clinical Research Experience
• Patient Care Management
• Protocol Compliance
• Registered Nurse License
• BLS Certification

• Clinical Trial Management
• Patient Recruitment
• Informed Consent Process
• Case Report Form Completion
• ICH Guidelines Knowledge

• Problem Solving
• Critical Thinking
• Training and Mentoring

• Registered Nurse License
• Basic Life Support (BLS)

• Clinical Trials
• Patient Safety
• Investigational Drug Administration
• Research Ethics
• Standard Operating Procedures