Medix · 2 weeks ago
Clinical Research Coordinator II/RN - 245578
Lone Tree, CO
Full-time
Onsite
Mid, Senior Level
3+ years expMedix is seeking a Clinical Research Coordinator II/RN to manage patient care in compliance with clinical trial protocols. The role involves screening patients, coordinating care, maintaining regulatory documents, and ensuring quality improvements in clinical research.
MedicalPharmaceuticalWholesale
Hiring Manager
Emma Housel
Responsibilities
Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on protocol
Coordinates patient care in compliance with protocol requirements. May disburse investigational drug and provide patient teaching regarding administration. Maintains investigational drug accountability. -In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings
Responsible for accurate and timely data collection, documentation, entry, and reporting. Schedules and participates in monitoring and auditing activities
Maintains regulatory documents in accordance with USOR SOP and applicable regulations
Participates in required training and education programs. Responsible for education of clinic staff regarding clinical research
May collaborate with Research Site Leader in the study selection process
Additional responsibilities may include working directly with other (non-USOR) research bases and/or sponsors
Identify quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality
May be responsible for compiling and reporting protocol activity, accrual data, and research financial information to practice administration and physicians
May oversee the preparation of orders by physicians to assure that protocol compliance is maintained. Communicates with physician regarding study requirements, need for dose modification, and adverse event reporting
Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law
Qualification
Required
Associate's degree in a clinical or scientific related discipline required
Minimum five years of experience in a clinical or scientific related discipline required, preferably in oncology
Graduate from an accredited program for nursing education (BSN preferred)
Minimum 3 years of nursing experience, preferably in oncology
Current licensure as a registered nurse in state of practice
Current BLCS or ACLS certification required
Preferred
Bachelor's degree preferred
SoCRA or ACRP certification preferred
Experience in clinical research preferred
OCN, SoCRA or ACRP certification preferred
Company
Medix
At Medix Distribution, we have designed solutions to meet the medical needs for the betterment of society as a whole.
11-50 employees
Funding
Current Stage
Early StageCompany data provided by crunchbase