Careers
The Ivy Culture
The Ivy Brain Tumor Center at Barrow Neurological Institute is a non-conventional, non-profit research program offering state-of-the-art clinical trials for patients with the most aggressive form of brain cancer. It is home to the largest collection of Phase 0 trials for brain tumors in the world. Each of our team members brings a unique set of skills and capabilities that helps make the Ivy Center a leading research facility for discovery and innovation. We are a community dedicated to accelerating drug development and precision medicine in neuro-oncology.
Our day-to-day interactions with patients, caregivers and each other are grounded in transparency: our conversations are always two-way, and our labs are open to ensure efficient collaboration. While we take incredible risks every day, the potential reward for patients is high. Everyone at the Ivy Brain Tumor Center is passionate about identifying and accelerating treatments that will make a meaningful difference in patients’ lives. Here, innovation never stops – we are open 24/7. At Ivy Brain Tumor Center, it’s our resilience that drove us to where we are today. Now, we are focused on progress – not process – so we can quickly bring promising therapeutic options to patients living with brain tumors around the world. Because for us, this work is personal.
Everyone here is passionate about what they are trying to accomplish. It’s not just a job.
Kendall FelixIvy Nurse Navigator
Help us find a cure
We are always looking for highly motivated and driven individuals to join our team. This is an opportunity to be a part of a national movement to rapidly identify new drugs that will save the lives of those battling advanced brain tumors. If this sounds like something you’d like to be a part of, view a list of our current job openings below.
Job Openings
Clinical Research RN
The Ivy Research Nurse Clinician plays an integral role for leading the coordination and management of the assigned protocols. Job duties will include screening potential patients for eligibility, providing study specific education to patients, families, and colleagues, conducting informed consent discussions and visits, and acting as a liaison with internal and external stakeholders involved in the clinical trial activities. Demonstrating knowledge and understanding of human research policies, regulations, procedures, and standards according to FDA, ICH/GCP guidelines is required. This position interacts with a variety of people, both internal and external, requiring exceptional communication skills. The ability to multi-task and remain organized in a high-volume clinical trial setting is required.
Interested?
If you don’t see a job listing relevant to your skillset, but are still interested in a career with us, please send your resume.
