Research Study Coordinator - Lead

Job ID 50456

The Department of Radiology is seeking an enthusiastic, detail-oriented individual to join our research coordinator and research management team.

Our research portfolio is expanding and includes NIH, industry, and foundation/internally sponsored research studies. The successful candidate will work closely with radiology faculty and staff to manage all aspects of our research projects including regulatory, study implementation and recruitment, data management and overall research operations.

Prior experience with clinical research is desired. Training will be provided and a willingness to learn is a must. This position will provide the successful candidate with very broad experience in many facets of research project coordination and management.

PRIMARY DUTIES AND RESPONSIBILITIES:

Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; obtains informed consent; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.

Routinely implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies, develops and completes study data collection forms and source documents; evaluates participants' progress in the study; documents, analyzes, investigates, and reports adverse events; resolves IRB/protocol management issues and recommends corrective action as appropriate, serves as liaison with funding or sponsoring agency.

Routinely ensures timely completion of all requirements (assessment, lab testing, procedures and treatments) to include scheduling and facilitating the patient's timely completion of protocol requirements. Collect and process research specimens in adherence with environmental health and safety protocols, review inventory of research supplies and check for expiration dates on a regular basis. Perform study required vital signs, specimen collection and processing, and any other study required procedures. Training will be provided on specific study related procedures. Assure research subject and staff safety at all times

Contribute to a positive, efficient, professional, and highly skilled research work environment. Initiate and engage in consistent communication and collaboration with clinic and department personnel and research leadership.

Create and maintain regulatory documentation and ensure regulatory compliance by research team. Complete IRB applications, amendments, personnel change forms, continuing review reports, and other study required documents. Complete clinical trial regulatory documents.

Acquire and use knowledge of institutional and federal regulations and guidelines related to research. Maintain compliance with Institutional and CITI training.

Other duties as assigned.

Salary Range: $50,367 - $91,392 annually
Grade: GGS - 010

A Bachelor's degree or an equivalent combination of education and relevant experience and at least 3 years of experience from which comparable knowledge and skills can be acquired is necessary.

To apply click https://apptrkr.com/5028461.