Research Coordinator II
About The Position
The University of Southern California (USC) Institute for Addiction Science is seeking an experienced clinical research coordinator to fill a full-time Research Coordinator II position. The successful candidate will contribute to single-site and multi-site clinical trials to evaluate treatments for substance use disorders, with a primary focus on pharmacotherapy studies, including GLP-1 receptor agonist medications. The successful candidate will be responsible for assisting with project management, participating in participant recruitment and screening; assisting with consenting and interviewing as needed; ensuring compliance with standard operating procedures; and assisting with data entry and data reporting tasks. The successful candidate will work closely with the principal investigator, pharmacists, students, and study participants to carry out study recruitment and data collection. The successful candidate will also assist with cross-site data collection for a multi-site clinical trial, including attending project meetings and contributing to coordinated execution of research procedures across sites. In addition to project-specific roles, the successful candidate will help to oversee general supervision of project staff and coordination of clinical research activities. The IAS Institute for Addiction Science is 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 position for two years, with eligibility for renewal contingent on availability of funds.
Requirements
- Demonstrated experience in clinical research coordinator roles (at least 2 years of relevant experience in a clinical research coordinator or similar role is required)
- Prior direct experience with recruitment of human participants for clinical trials is required
- Demonstrated experience supervising research project staff is required
- Documentation of certified research coordinator training is required
- A bachelor’s degree or higher is required
- Strong computer skills
- Demonstrated experience with data collection and clinical trial management software (e.g., REDCap)
- Ability to work in a fast-paced clinic/hospital environment while interacting with participants/patients and multidisciplinary team members
- Administrative or research experience
- Knowledge of medical environment and terminology
- Knowledge and understanding of federal, state, and institutional research regulations as well as Good Clinical Practices (GCP) and HIPPA regulations
- Proficient with MS Office applications
- Demonstrated effective communication and writing skills
- Ability to multi-task
- Demonstrated ability to work as part of a team as well as independently
Nice To Haves
- 3 or more years of relevant experience in a clinical research coordinator or similar role is preferred
- Experience with managing and planning project budgets is preferred
- Knowledge of medical environments and medical terminology is preferred
- Phlebotomy certification and CA State Phlebotomy License is preferred
- Demonstrated experience in clinical research assistant/coordinator positions on clinical trials
- Staff education and orientation experience
- Knowledge of Electronic Data Capture (EDC) systems and Clinical Trial Management Systems (CTMS)
Responsibilities
- Assisting with project management
- Participating in participant recruitment and screening
- Assisting with consenting and interviewing as needed
- Ensuring compliance with standard operating procedures
- Assisting with data entry and data reporting tasks
- Working closely with the principal investigator, pharmacists, students, and study participants to carry out study recruitment and data collection
- Assisting with cross-site data collection for a multi-site clinical trial, including attending project meetings and contributing to coordinated execution of research procedures across sites
- Overseeing general supervision of project staff and coordination of clinical research activities
- Co-lead coordination of clinical research projects in collaboration with members of a multidisciplinary team
- Assisting with administrative and literature review tasks as needed
Benefits
- Excellent benefits and perks
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
