The RN Clinical Trials Coordinator 3 (RN CTC3) 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 CTC3 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 CTC3 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.
- Working with physicians in-person and virtually at LSUHSC clinics, various satellite locations, and with our partner institutions.
Minimum Qualifications
Required Education: BSN or RN
Certifications/Licenses Required: Valid license to practice as a Registered Nurse in Louisiana.
Minimum years required: Five years of clinical RN experience.
Preferred Qualifications:
Preferred Experience: RN experience inclusive of Oncology, clinical trials, and/or surveillance/auditing experience. Data Management experience.
#J-18808-Ljbffr
