Medix
Clinical Research Nurse
Medix, Phila, Pennsylvania, United States, 19117
We are looking for a self-starter to join our team as a
Registered Nurse.
We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. As a
Clinical Research Nurse
with our esteemed organization, you will be at the forefront of cutting-edge
cancer
research that can positively impact patient outcomes. Join us in our mission to advance medical knowledge and make a difference in the lives of patients in the
Philadelphia area
and beyond.BENEFITS4:1
hybrid
schedule allowing for 1 day remote per week!Medical, Dental, Vision insuranceDirect hire, permanent rolePTO and paid holidays401k with employer matchMental Health Assistance, Gym Discounts, Referral Program
and more!RESPONSIBILITIESIn conjunction with Clinical Research Associate, schedules and attends Study Initiation Visits, Monitor Visits, and coordinate meetings to ensure all appropriate disciplines in attendance.Assists institutional investigators with identification of potential research participants for the actively accruing clinical trials-prescreening.Serves as a resource during site visits/audits by the, FDA, NCI,Pharmaceutical firms, or other agencies designated by sponsors (especially as related to appropriate consent, proper record keeping and quality assurance).Alerts investigators and appropriate personnel of communications regarding adverse drug reaction reports.Checks eligibility requirements to determine research participant eligibility for assigned studies.Registers all research participants according to sponsor requirements.Monitors through various forms of communication research participants for toxicities of protocol treatment.Documents research participant toxicities for clinic visits or phone interviews in compliance with applicable OCR SOP/SWP.Provides source documentation in the research participant's study chart as appropriate.Provides research participant/family members with instructions and education regarding the specific clinical research protocol(s) presented to them.Creates protocol specific scheduling templates in scheduling in EPIC and schedules tests appropriately. Follows-up to ensure that all required tests, procedures or treatments were scheduled and completed as ordered.Prepares and submits reports of serious adverse events as required by theprotocol, sponsor, IRB, FDA, NCI and OCR standard operating/work procedures in appropriate and timely fashion.Ensures that all baseline tests required by protocol are performed within specified timeframe and all eligibility requirements are met.Ensures adherence to the clinical research protocol and that all protocoldeviations are documented carefully and submitted correctly and promptly.Monitors dosage modifications and treatment calculations in conjunction with treating physician and Investigator.Assists Protocol Support Lab with arrangements for collection and shipping of samples as required by protocol.Assists with completion of outstanding queries and case report forms as needed.Prepares and attends close out meeting with sponsor.In conjunction with Clinical Research Associate, obtains and radiology reports/scans, operative reports, or other specialized reports as needed for protocol purposes.
Registered Nurse.
We are looking for someone to take ownership of their clinical studies and who can work autonomously to problem solve and stay organized. As a
Clinical Research Nurse
with our esteemed organization, you will be at the forefront of cutting-edge
cancer
research that can positively impact patient outcomes. Join us in our mission to advance medical knowledge and make a difference in the lives of patients in the
Philadelphia area
and beyond.BENEFITS4:1
hybrid
schedule allowing for 1 day remote per week!Medical, Dental, Vision insuranceDirect hire, permanent rolePTO and paid holidays401k with employer matchMental Health Assistance, Gym Discounts, Referral Program
and more!RESPONSIBILITIESIn conjunction with Clinical Research Associate, schedules and attends Study Initiation Visits, Monitor Visits, and coordinate meetings to ensure all appropriate disciplines in attendance.Assists institutional investigators with identification of potential research participants for the actively accruing clinical trials-prescreening.Serves as a resource during site visits/audits by the, FDA, NCI,Pharmaceutical firms, or other agencies designated by sponsors (especially as related to appropriate consent, proper record keeping and quality assurance).Alerts investigators and appropriate personnel of communications regarding adverse drug reaction reports.Checks eligibility requirements to determine research participant eligibility for assigned studies.Registers all research participants according to sponsor requirements.Monitors through various forms of communication research participants for toxicities of protocol treatment.Documents research participant toxicities for clinic visits or phone interviews in compliance with applicable OCR SOP/SWP.Provides source documentation in the research participant's study chart as appropriate.Provides research participant/family members with instructions and education regarding the specific clinical research protocol(s) presented to them.Creates protocol specific scheduling templates in scheduling in EPIC and schedules tests appropriately. Follows-up to ensure that all required tests, procedures or treatments were scheduled and completed as ordered.Prepares and submits reports of serious adverse events as required by theprotocol, sponsor, IRB, FDA, NCI and OCR standard operating/work procedures in appropriate and timely fashion.Ensures that all baseline tests required by protocol are performed within specified timeframe and all eligibility requirements are met.Ensures adherence to the clinical research protocol and that all protocoldeviations are documented carefully and submitted correctly and promptly.Monitors dosage modifications and treatment calculations in conjunction with treating physician and Investigator.Assists Protocol Support Lab with arrangements for collection and shipping of samples as required by protocol.Assists with completion of outstanding queries and case report forms as needed.Prepares and attends close out meeting with sponsor.In conjunction with Clinical Research Associate, obtains and radiology reports/scans, operative reports, or other specialized reports as needed for protocol purposes.