Apply on Employer Site

The US Oncology Network · 22 hours ago

Clinical Research Coordinator - Twain

LV Metro Area

Full-time

Onsite

Entry Level

1+ years exp

The US Oncology Network is dedicated to advancing cancer care through clinical research. They are seeking a Clinical Research Coordinator responsible for managing and coordinating tasks for multiple clinical research studies, ensuring protocol compliance, and collecting clinical trial data.

CommunitiesHealth CareMedicalOncologyTest and Measurement

Responsibilities

Under direct supervision of a physician and nurse (if applicable), is responsible for enlisting, maintaining, and assuring protocol compliance for all patients on clinical trials

Collaborates with physicians in determining the eligibility of patients for clinical trials

Ensures site research quality by practicing in compliance with Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP), and applicable federal, state, and local regulations

Screens potential patients for protocol eligibility; Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients in protocol

Coordinates patient care in compliance with protocol requirements. May disburse investigational drugs 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, and 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 by SOPs 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 research bases and/or sponsors

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

Clinical researchClinical Practice (GCP)Standard Operating Procedures (SOP)Oncology experienceSoCRA certificationACRP certificationData collectionPatient care coordinationMedical office experiencePatient confidentiality