Are You Radiant?

We’re always looking for new talent! Below you’ll find our current career opportunities.

Career Opportunities

Radiant Research is seeking a Regulatory Compliance Associate to be responsible for all aspects of regulatory compliance and documentation, quality assurance, auditing, as well as organizational training related to GCP and SOP compliance. The position will work in our Dallas, TX out-patient research facilities. The position will be responsible for all aspects of regulatory compliance and documentation, […]

Radiant Research is seeking a Research Assistant in Atlanta, GA! The Research Assistant (RA), as delegated by the Site Manager, executes daily clinical research activities according to the company’s SOPs, GCP and FDA/ICH guidelines. Executes informed consent process and monitors patient status; collects and organizes research data; The Research Assistant must also be able to […]

Radiant Research is seeking a Research Assistant in Akron, OH! The Research Assistant (RA) executes daily clinical research activities (according to the company’s SOPs, GCP and FDA/ICH guidelines), executes informed consent process and monitors patient status, and collects and organizes research data.   The Research Assistant must also be able to perform clinical tasks (i.e. phlebotomy, EKGs, vital […]

We are currently seeking an Accounts Payable Supervisor who will support the Accounting/Finance department.  Job duties will include processing invoices (AP), cash balances, bank reconciliations, receipts, check register/input, cost accounting duties, completing related documentation and reporting functions, as well as supervisory duties, staff oversight and training.  Specifically the candidate will be responsible for: 1. Performing corporate accounting […]

Radiant Research, Inc. has an immediate opportunity for an Accounting Associate for our Tempe, AZ corporate office! Job duties will include processing invoices (AP), cash balances, bank reconciliations, receipts, check register/input, cost accounting duties, completing related documentation and reporting functions.  Specifically you will be responsible for: 1. Performing corporate accounting functions including bank reconciliations, cash balances, receipts, check register/input, etc. […]

Radiant Research is currently seeking a Clinical Research Coordinator for our site in Vista, California! The Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to CRA’s SOPs, GCP and FDA/ICH guidelines. In this role you will ensure IRB approved protocols are implemented and followed; execute the informed […]

Radiant is currently seeking a Sr. Clinical Research Coordinator for our site in Dallas, TX! The Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to CRA’s SOPs, GCP and FDA/ICH guidelines. In this role you will ensure IRB approved protocols are implemented and followed; execute the informed […]

Radiant Research is currently seeking a Clinical Research Coordinator in Atlanta, GA! The Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to CRA’s SOPs, GCP and FDA/ICH guidelines. In this role you will ensure IRB approved protocols are implemented and followed; execute the informed consent process and […]

Radiant Research is seeking a Research Assistant in Dallas, TX!   The Research Assistant (RA), as delegated by the Site Manager, executes daily clinical research activities according to the company’s SOPs, GCP and FDA/ICH guidelines. Executes informed consent process and monitors patient status; collects and organizes research data; The Research Assistant must also be able to perform […]

Radiant Research is seeking a Research Assistant in Oklahoma City, OK!   The Research Assistant (RA), as delegated by the Site Manager, executes daily clinical research activities according to the company’s SOPs, GCP and FDA/ICH guidelines. Executes informed consent process and monitors patient status; collects and organizes research data; The Research Assistant must also be able to […]

Radiant Research is currently seeking a Clinical Research Coordinator in Dallas, TX! The Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to SOPs, GCP and FDA/ICH guidelines. Ensures IRB approved protocols are implemented and followed. Executes informed consent process and monitors patient status and safety; collects and organizes […]

Radiant Research is seeking 3 Research Assistants in the Omaha, NE area!   Our offices are located in Council Bluffs, IA, Elkhorn, NE and Fremont, NE! The Research Assistant (RA), as delegated by the Site Manager, executes daily clinical research activities according to the company’s SOPs, GCP and FDA/ICH guidelines. Executes informed consent process and monitors patient […]

Radiant Research, Inc. has an immediate opportunity for an Administrative Assistant (Quality Assurance and Training) at our Tempe, AZ corporate office! This position assists with essential duties within the Quality Assurance and Training Departments, including preparation of documents and assisting with responses to site staff members.  Incumbent must be able to work in a very busy interactive environment […]

Radiant Research is seeking a Patient Recruitment Specialist in Chandler, AZ! In this position you will be responsible for the recruitment of appropriate study participants into clinical research protocols. This will require maintaining the patient database, medical history review to determine eligibility, phone screening, community outreach and other recruitment activities including, the coordination and tracking […]

Radiant Research is seeking 2 Research Assistants in Las Vegas, NV! The Research Assistant (RA), as delegated by the Site Manager, executes daily clinical research activities according to the company’s SOPs, GCP and FDA/ICH guidelines. Executes informed consent process and monitors patient status; collects and organizes research data; The Research Assistant must also be able […]

Radiant Research is seeking a Site Manager in Council Bluffs, IA! The Site Manager (SM) provides on-site, daily leadership with the execution and coordination of clinical research activities according to the company’s SOPs, ICH/GCP and FDA guidelines. The SM oversees the daily activities of the clinical research coordinators and assistants to ensure smooth site operations […]

Radiant Research is currently seeking a Sr. Clinical Research Coordinator in Denver, CO! The Sr. Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to the company’s SOPs, GCP and FDA/ICH guidelines. In this role you will ensure IRB approved protocols are implemented and followed; execute the informed consent […]

Radiant Research is currently seeking a Clinical Research Coordinator for our site in Council Bluffs, IA! The Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to the company’s SOPs, GCP and FDA/ICH guidelines. In this role you will ensure IRB approved protocols are implemented and followed; execute […]

Radiant Research is seeking a Clinical Research Coordinator in Vista, California! The Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to SOPs, GCP and FDA/ICH guidelines. Working under the direction of the principal investigator, the CRC’s responsibilities include: Becoming thoroughly familiar with the protocol, case report […]

Radiant Research is seeking a Clinical Research Coordinator in Fremont, Nebraska! The Clinical Research Coordinator (CRC), as delegated by the principal investigator, executes and coordinates daily clinical research activities according to CRA’s SOPs, GCP and FDA/ICH guidelines. In this role you will ensure IRB approved protocols are implemented and followed; execute the informed consent process and monitor […]