The US Oncology Network
Location
Columbia, Missouri
The Clinical Research Assistant is responsible for recruiting, screening, and enrolling patients in clinical trials while ensuring strict protocol compliance. They coordinate subject visits, maintain regulatory documentation, and collaborate with physicians to document patient responses and adverse events.
An associate's degree in a clinical or scientific discipline is required, with a bachelor's degree and SoCRA or ACRP certification preferred. Candidates should have 1-2 years of experience in a clinical/scientific field and strong communication and organizational skills.
30-4:00 Missouri Cancer Associates is a multi-specialty practice including medical oncology, hematology, radiation oncology, and urology. We have 22 providers that service ten Missouri communities. Our main office is in Columbia. Through state-of-the-art medical technology, highly experienced physicians and nurse practitioners and quality patient care, Missouri Cancer Associates has become the premier Cancer Treatment Center in Mid-Missouri. In 2022, we celebrated our 40th year of taking care of patients! Candidates should have an outgoing and friendly demeanor, a positive work ethic, and have a track record of working well with others in a team environment. We prefer applicants who have customer service experience. You must exemplify the values of our company and provide our patients with the highest levels of care This position is located at 1705 E Broadway Columbia, Missouri. Missouri Cancer Associates is affiliated with Urology Associates of Central Missouri and the US Oncology Network.
The Clinical Research Assistant is responsible for recruiting, pre-screening, screening, consenting, and enrolling patient in clinical trials. Clinical Research Assistant also coordinates and oversees the subject’s visits in accordance with the protocol requirements. Duties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers. Acts as resource for the education and training of clinic staff as well as resource for problem solving of complex issues for the implementation of the research process throughout the clinic, process improvements and SOPs. Compiles and reports protocol activity; accrual data, and financial information. Assures site research quality by practicing in compliance with "The Network" Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA. Supports and adheres to "The Network" Compliance Program, to include the Code of Ethics Business Standards.
Associate's degree in a clinical or scientific related discipline required, bachelor’s degree preferred. Minimum 1-2 years of experience in a clinical or scientific related discipline SoCRA or ACRP certification preferred. Experience in Microsoft Office Experience working with physicians preferred Experience working in clinical research is preferred Must have excellent communication skills Excellent organizational skills Strong ability to multi-task Excellent time management skills Must have strong interpersonal skills to be able to interact with multiple people on many different levels Must have a high level of attention to detail Must be able to work in a fast-paced environment May be responsible for basic clinical assessments Traditional office environment
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