- Knowledge of disease process, standard or care, and oncologic terminology
- Knowledge of study protocol, inclusion and exclusion criteria and amendment training, study endpoints, reportable events (Adverse Event, Serious Adverse Event, Adverse Events of Special Interest)
- Define methods of subject identification and recruitment
- Weekly review of study visits completed, Electronic Data Capture (EDC) entries
- Weekly review of study status
- Conduct subject recruitment and confirm subject eligibility
- Assists in recruitment efforts, contacting and identifying potentially eligible participants to screen
- Coordinate study presentation and Informed Consent Form process with Co-Investigator; obtain consents for amendments where applicable
- Scheduling and completion of all protocol required study visits and procedures
- Preparation and maintenance of source documents and review with investigator
- Maintain Investigational Product dispensing and accountability
- Review Adverse Events and Serious Adverse Event with Primary Investigator within 24 hour of event report to Institutional Review Board (IRB) and sponsor.
- Subject retention activities and follow up procedures
- Protocol monitoring activities, preparation, data clarification
- Coordination of assessment by investigator of patient, lab results and procedure findings to ensure safe and appropriate enrollment in study and prior to all treatments
- Vital sign assessments, conduction of ECG, specimen collections, phlebotomy, IV and port insertion, treatment and removal, injections
- Initiating chemotherapy infusions, maintenance and monitoring of infusion, and observation post infusion
- Your accuracy and attention to detail is second to none
- You are able to prioritize tasks and adapt to incoming needs
- You keep information organized well documented
- You have a good internal clock and manage your time well
- You communicate early and often to the Principal Investigator, your supervisor, and peers
- You are empathetic, caring, and relatable
- You have a way of putting your patient's at ease
- You have the dual ability of being task and relationship focused
- Licensed as a registered nurse (RN) in MO
- Oncology certification and minimum one year of experience as an RN in a clinical setting
- Your preferred experience:
- Experience with chemotherapy administration
- Clinical Research Coordinator experience preferred. Certification of Clinical Research Coordinator, preferred. If no certification, award of certification within two years.
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Clinical Research Nurse - Fenton, United States - Medix™
Description
Licensed as a Registered Nurse (RN) in the state of Missouri.
Must have oncology experience.
Onsite: Monday through Friday 8AM-5PM CST
Benefits: Health, Vision, Dental, 401K, etc.
As our Oncology Nurse Coordinator will be responsible for coordinating, facilitating, and monitoring the implementation of research study protocols being conducted in accordance with departmental policy, institutional policy, sponsor requirements, and FDA regulations, specific to oncology protocols. You will also provide, manage, and coordinate care for patients participating in oncology clinical trials, including investigational product and standard of care therapy.
What you'll be responsible for:
Who you are:
Your qualifications:
