At the Cancer Center of Kansas, we value each and every employee for their life-saving expertise and the role they play in making our patients’ lives as easy and comfortable as possible. Our employees are our most valuable resource. They help us create the warm and caring environment that’s the foundation for some of the best cancer research and care in the country. If you would like to join a team dedicated to improving lives every day, contact us below.
For employment opportunities, please contact:
Cancer Center of Kansas Human Resources
Phone: (316) 613-4203 Fax: (316) 613-4290
If you have interest, you are welcome to apply by submitting your resume in conjunction with the below CCK Application form via fax. Otherwise, please call the above contact for information on how to submit your resume and application electronically.
Full-Time (40 hours): To conduct research studies according to protocol and regulatory requirements. The ultimate goal of the Research Nurse is to protect the patients who participate in research studies. The Research Nurse also promotes good clinical practices within the research team.
Full-time (40 hours): Qualified RN, with good IV skills to administer chemotherapy in an outpatient, busy, multi-physician oncology practice in Wichita, KS. Assures correct medication dosage form, strength, and quantity as per physician order. Assesses patients for current condition, including labs, and side effects from current therapy. New graduates are welcome to apply.
Full-time (40 hours): Responsible for greeting patients and visitors into the clinic in a prompt, courteous, and professional manner. Acts as the Patient Ambassador, making sure patients are checked in and out using our scheduling system, and are delivered to their appropriate appointment. Serves as liaison between patient and other care staff. Previous medical office or reception experience preferred.
Full-time (40 hours): Responsible for the regulatory component of Pharmaceutical Research. The person in this position works with various Institutional Review Boards (IRBs), which are the agencies that specify how each clinical trial will be regulated. The person in this position will prepare and maintain regulatory documents pertaining to each Pharmaceutical study being considered or already approved. Excellent written, oral communication and organizational skills are required. Experience in a medical office or research area is preferred.
Please call 316-268-1248 to make an appointment.
