RN Clinical Trials Coordinator 2

Louisiana State University Health Sciences Center Portal • New Orleans, LA

2d

About The Position

The RN Clinical Trials Coordinators (RN CTC ) will coordinate, manage, and assist physicians in enrolling and monitoring patients on all Phase I drug-industry sponsored and the NCI -funded clinical trials for the LSUHSC Cancer Center. The RN CTCs will recruit, enroll, administer care, and provide patient follow-up visits in-person and virtually on all NCI and pharmaceutical sponsored studies associated with the Cancer Center and its partner institutions. Duties will include: attending oncology clinics in-person and virtually to collaborate with physicians to determine patient eligibility; informing and educating the patient and their families about a particular study; providing informed consent; scheduling regular appointments and follow-up as needed; providing treatment; obtaining study specific lab-work; evaluating and monitoring effects of treatment; organizing, collecting and managing data; submitting forms and reports as required; working closely with monitors from the drug companies to ensure protocols are being implemented correctly and that the necessary clinical data is being captured; processing and packaging specimens for mail-out; attending regular toxicity meetings with sponsors and physicians. The RN CTC will work with physicians in-person and virtually at LSUHSC clinics, various satellite locations, and with our partner institutions.

Responsibilities

• Coordinate, manage, and assist physicians in enrolling and monitoring patients on clinical trials
• Recruit, enroll, administer care, and provide patient follow-up visits in-person and virtually
• Attend oncology clinics in-person and virtually to collaborate with physicians to determine patient eligibility
• Inform and educate patients and their families about studies
• Provide informed consent
• Schedule regular appointments and follow-up as needed
• Provide treatment
• Obtain study specific lab-work
• Evaluate and monitor effects of treatment
• Organize, collect, and manage data
• Submit forms and reports as required
• Work closely with monitors from drug companies
• Process and package specimens for mail-out
• Attend regular toxicity meetings with sponsors and physicians

What This Job Offers

• Job Type: Full-time
• Education Level: No Education Listed
• Number of Employees: 1,001-5,000 employees