Research Coordinator Supervisor

Overview

The University of Southern California Institute for Addiction Science is seeking an experienced clinical research coordinator to fill a full-time Research Coordinator Supervisor position. The successful candidate will play a central role in the management of single-site and multi-site clinical trials to evaluate new treatments for addiction, with a primary focus on GLP-1 receptor agonist medications. The candidate will assume a central leadership and project management role on numerous project-specific activities, including coordinating participant recruitment, supervising study research staff, interviewers and consenters; assisting with consenting and interviewing as needed; overseeing compliance with protocols and standard operating procedures; and assisting with Institutional Review Board and regulatory compliance. The candidate will communicate and work closely with the site PIs, research coordinators, clinicians, pharmacists, students, and study participants. The successful candidate will also assume general project management roles for a multi-site clinical trial, including coordinating research activities and project meetings, ensuring compliance with staff training / certifications, and ensuring coordinated execution of research procedures across sites. The candidate will collect ongoing data on the success of engaging participants so that research participation can be optimized across study sites. In addition to project-specific roles, the successful candidate will help to oversee general supervision of project research staff, students, and volunteers in the coordination of various lab activities.

This position is funded through the IAS Institute for Addiction Science, the nation's first university-wide, transdisciplinary addiction science institute. IAS scientists include 80 faculty members from 10 different USC schools. This position will be based in the Biobehavioral Addiction Research Lab (BARLab), located on the Health Sciences Campus. The position is funded by sponsored research projects and will be a full time, staff position for 3 years and is eligible for renewal based on availability of funds.

Job Accountabilities

The successful candidate will work in a clinical research setting and will have extensive prior experience working with study participants and / or patients, and prior experience coordinating research projects with members of a multidisciplinary team. Other important qualifications include strong computer skills, demonstrated experience with data collection and clinical trial management software, and the ability to work in a fast-paced clinic / hospital environment while interacting with participants / patients and multidisciplinary team members. This position requires strong attention to detail, excellent communication skills, the ability to ensure timely progress toward recruitment milestones and project objectives, the ability to take on and follow through with tasks autonomously. Applicants with a strong research background in the clinical / medical sciences, and with professional experience in a university research environment, are encouraged to apply.

Required Qualifications

• Demonstrated experience in clinical research coordinator roles (including at least 5 years of relevant experience in a clinical research coordinator or research manager role involving recruitment of human participants);
• Demonstrated experience supervising research project staff;
• Documentation of certified research coordinator training;
• Experience with managing and planning project budgets;
• Knowledge of medical environments and medical terminology;
• Master's degree (or higher) required for this position.

Preferred Qualifications

Salary and Education

The expected annual base salary range for this position is $89,000 - 112,000. Minimum Education : Master's degree; Minimum Experience : 5 years; Knowledge and understanding of federal, state, and institutional research regulations including Good Clinical Practices (GCP) and HIPAA regulations. Proficient with MS Office; experience with Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS).

Employment Details

Note : This posting includes references to related USC roles and alerts but does not alter the original job information or requirements.

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