Make a Difference Where Research Meets Hope.
Join a privately owned oncology practice where innovation, compassion, and patient-centered care come together. As our Clinical Research Supervisor, you will lead groundbreaking clinical trials that bring tomorrow's cancer treatments to patients today, while shaping a high-performing research program dedicated to improving lives and advancing the future of oncology.
Highlands Oncology began in 1996 with three physicians and a desire to change the face of oncology care in our community. Dr. Malcolm Hayward, Dr. Dan Bradford, and Dr. Thad Beck knew that patients do better at home, in the community where they live and work, and where their support system is already in place. In furthering that goal, Highlands has grown with the region from a single location 26 years ago, to 6 locations in Northwest and Northcentral Arkansas today employing more than 800 diverse team members.
As Northwest Arkansas continues to grow, so must the services and providers available in the region. Highlands Oncology is committed to remaining on the cutting edge to ensure our community has access to the very best cancer care. What we have is something quite unique right here in our own backyard with a caring multidisciplinary team focused on treating patients like family.
Job Summary: The clinical supervisor oversees the research staff, ensuring all department and Highland’s policies are being followed, while also managing any personnel issues that arise.
Supervisory Responsibilities:
- Manage day-to-day operation of the research department to ensure an efficient and effective department.
- Supervise staff members, act as back-up when necessary.
- Assess employee performance.
- Coordinate department meetings.
- Oversee quality assurance for the department.
- Assist staff when needed.
- Monitor work/patient flow between the departments.
Job Duties / Responsibilities (may include those of a Clinical Research Coordinator as follows):
- Must learn and be proficient in the use of the practice EMR and practice management programs.
- Act as a resource to hospital and clinic personnel/physicians regarding research activity.
- Screens potential study patients according to protocol inclusion/exclusion criteria.
- Meets with study subjects and schedules their visits according to protocol requirements.
- Reports all adverse events to the Principal Investigator and sponsor.
- Obtains and completes data for study subjects and/or work with the Research Data Manager to ensure subject data is collected according to the study.
- Completes case reports and maintains records of each study subject and/or work with the Research Data Manager to ensure data is entered into the electronic data capture (EDC) system according to study.
- Will meet with Clinical Research Associates and sponsor representatives.
- Works with Investigators, mid-level providers, nurses, and other Clinical Research Coordinators to identify/document toxicity, adverse events, etc.
- Acts as a resource to hospital and clinic personnel/physicians regarding research activity.
- Limited travel may be required for investigator meetings, educational opportunities, and between Fayetteville, Springdale, and Rogers clinics.