Clinical Research Coordinator / Oncology

The US Oncology Network•Columbia, MO

5d•Onsite

About The Position

As a Clinical Research Coordinator I, you will play a pivotal role in the management and coordination of multiple clinical research studies. Your responsibilities will include patient screening for eligibility, participation in study visits, and ensuring protocol compliance. You will collaborate with physicians and other healthcare providers to conduct ongoing assessments and documentation, ensuring adherence to US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), Good Clinical Practice (GCP) principles, and applicable regulations.

Requirements

Associate degree in a clinical or scientific discipline required; Bachelor’s degree preferred.
Minimum of one year of experience in a clinical or scientific discipline, oncology experience preferred.
Proficiency in Microsoft Office.
Exceptional communication and organizational skills.
Strong multitasking and time management abilities.
Attention to detail and interpersonal skills for interacting with diverse individuals.
Ability to perform basic clinical assessments.
Extensive computer-based work.
Standing and walking for significant periods.
Occasionally lifting items up to 40 lbs.
Normal range vision and hearing required.

Nice To Haves

Bachelor’s degree preferred.
Oncology experience preferred.
Experience working with physicians is preferred.

Responsibilities

Screen and evaluate potential patients for protocol eligibility.
Present trial concepts and details to patients and facilitate the informed consent process.
Assist in patient care in accordance with protocol requirements, including investigational drug disbursement and accountability.
Participate in data collection, entry, and reporting.
Collaborate with physicians to monitor patient conditions, adverse events, and study drug responses.
Engage in required training, education, and auditing activities.
Assist with regulatory document maintenance and lab specimen logistics.