Cancer Treatment Centers of America® (CTCA®) takes a unique and integrative approach to cancer care. Our patient-centered care model is founded on a commitment to personalized medicine, tailoring a combination of treatments to the needs of each individual patient.
At the same time, we support patients' quality of life by offering therapies designed to help them manage the side effects of treatment, addressing their physical, spiritual and emotional needs, so they are better able to stay on their treatment regimens and get back to life.
At the core of our whole-person approach is what we call the Mother Standard® of care, so named because it requires that we treat our patients, and one another, like we would want our loved ones to be treated. This innovative approach has earned our hospitals a Best Place to Work distinction and numerous accreditations. Each of us has a stake in the successful outcomes of every patient we treat.
The oversight of all research nurses, research coordinators, and data coordinators
The oversight of clinical research operations under the direction of the research director
Assisting and overseeing the compliance of policies and procedures, SOPs, SWIs and FDA regulations as they pertain to research
Maintaining a standard of excellence and remain knowledgeable about operational changes within the hospital and CTCA Clinical Research, Inc.
Ensuring all clinical trials for Tulsa, CCRC are followed and managed appropriately for proper billing and invoicing to ensure maximum revenue for the department.
This position will work closely with other department supervisors and/or directors within the hospital to create better processes and ensure that research operations are integrated into normal workflows.
Bachelor's degree in a healthcare or business-related field with healthcare experience (Business Administration, Health Care Administration, clinical field (science, health, medicine, pharmacy, nursing), OR equivalent experience
minimum of 2 years of hospital experience
Certification through SoCRA, ACRP, or other reputable entity within 3 years
Basic Life Support training within 6 months
Human Subjects Protection training/certification within 90 days
Availability for off-hours coverage and occasional travel
Basic Oncology class within 1 year of employment
3+ years of research experience
3+ years of clinical oncology experience
Master's degree in a healthcare or business-related field with healthcare experience (Business Administration, Health Care Administration, clinical field (science, health, medicine, pharmacy, nursing)
Certification through Society of Clinical Research Associates, Association of Clinical Research Professionals, or other reputable entity
Phase I clinical research experience
Lifting of up to 10 lbs
We win together
Each CTCA employee is a Stakeholder, driven to make a true difference and help win the fight against cancer. Each day is a challenge, but this unique experience comes with rewards that you may never have thought possible. To ensure each team member brings his or her best self, we offer exceptional support and immersive training to encourage your personal and professional growth. If you're ready to be part of something bigger and work with a passionate, dynamic group of care professionals, we invite you to join us.