Clinical Research Coordinator at US Oncology, Inc. Tyler, TX

Benefits

Qualifications

• •Clinical Research Coordinator role?will have the following background and experience:
• •Minimum one year of experience in a clinical or scientific related discipline, preferably in oncology required
• •Level 2 (in addition to level 1 requirements)
• •Minimum three years of experience in a clinical or scientific related discipline required, preferably in oncology
• •Level Sr (in addition to level 1 and 2 requirements)
• •Minimum five years of experience in a clinical or scientific related discipline required
• •The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job
• •Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
• •Requires standing and walking for extensive periods of time
• •Requires corrected vision and hearing to normal range
• •Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment
• •8 more items(s)

Responsibilities

• •Responsible for supporting the management and coordination of tasks for multiple clinical research studies to include screening patients for eligibility and participates in the subject's study visits and required activities per protocol
• •Duties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers, and participation in required training and education, Assures site research quality by practicing in compliance with US Oncology Research, Inc
• •(USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA
• •Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards
• •Screens potential patients for protocol eligibility.?
• •Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials
• •Assists with patient care in compliance with protocol requirements.?
• •May disburse investigational drug and maintain investigational drug accountability.?
• •Participates in data collection, entry, and reporting for the subjects
• •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
• •Participates in required training and education programs as well as monitoring and auditing activities
• •May work directly with sponsors
• •May participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite
• •Assists with collection and maintenance of regulatory documents in accordance with USOR SOPs and applicable regulations
• •May assist in the packing and shipping of lab specimens to central vendors
• •May be required to complete Hazmat and/or IATA training
• •Occasionally lifts and carries items weighing up to 40 lbs
• •Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions
• •15 more items(s)