RN - Clinical Trials Coordinator Senior

Louisiana State University Health Sciences Center PortalNew Orleans, LA
4d

About The Position

The RN Clinical Trials Coordinator Senior (RN CTC ) will coordinate, manage, and assist physicians in enrolling and monitoring patients on all drug-industry sponsored and the NCI -funded clinical trials for the LSUHSC Cancer Center. The RN CTC 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, the Genitourinary Oncology team, Gynecologic Oncology team, and its partner institutions. The RN CTC will also work with the Virtual Research clinical trials program which offers specialized care to female patients which would otherwise be unattainable for most women in Louisiana. 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. 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 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
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