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.

BENEFITS

• 4:1 hybrid schedule allowing for 1 day remote per week!
• Medical, Dental, Vision insurance
• Direct hire, permanent role
• PTO and paid holidays
• 401k with employer match
• Mental Health Assistance, Gym Discounts, Referral Program and more!

RESPONSIBILITIES

• In 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 the
• protocol, 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 protocol
• deviations 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.