Clinical Non-Licensed Pool/Clinical Research Coordinator - Diverse Lynx
Los Angeles, CA 90048
About the Job
Location: 8631W. 3rd Street, Suite 635E, Los Angeles, CA 90048
Required:
* 1 year of clinic research experience
Preferred:
* Cardiology experience
* Vascular experience
* Epic/CS Link experience
Primary Duties and Responsibilities
" Establishes and executes logistical aspects of clinical research projects to achieve project objectives,
including project planning, projecting resource requirements, and developing systems to ensure protocol
compliance and patient safety.
" Coordinates administrative functions of research studies, including scheduling of patients for research visits,
procedures and labs and completion and maintenance of consent forms, case report forms, SAE s and source
documents.
" Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical
trial concepts and details to the patients, and supporting the informed consent process.
" Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution
of queries from sponsors or regulatory entities.
" Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study
monitoring and designs and implements needed corrective actions.
" Responsible for compiling and reporting on each study including information related to protocol activity,
accrual data, workload, and other research information; present this information at regular research staff
meetings.
" Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and Safety
Letters in accordance with local and federal guidelines.
" Identifies quality and performance improvement opportunities and collaborates with staff in the development
of action plans to improve quality.
" Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical
research efficiency as needed.
" Provides technical support for the preparation of grant proposals, publications, presentations and special
projects.
" Provides assistance with research project budget development, including identifying and classifying routine
care vs. research related care and provides assistance with research participant research billing and
reconciliation.
Required:
* 1 year of clinic research experience
Preferred:
* Cardiology experience
* Vascular experience
* Epic/CS Link experience
Primary Duties and Responsibilities
" Establishes and executes logistical aspects of clinical research projects to achieve project objectives,
including project planning, projecting resource requirements, and developing systems to ensure protocol
compliance and patient safety.
" Coordinates administrative functions of research studies, including scheduling of patients for research visits,
procedures and labs and completion and maintenance of consent forms, case report forms, SAE s and source
documents.
" Responsible for screening and recruitment of potential patients for protocol eligibility, presenting non-medical
trial concepts and details to the patients, and supporting the informed consent process.
" Responsible for accurate and timely data collection, documentation, entry and reporting, including resolution
of queries from sponsors or regulatory entities.
" Coordinates institutional, pharmaceutical and internal audits, including facilitating third party study
monitoring and designs and implements needed corrective actions.
" Responsible for compiling and reporting on each study including information related to protocol activity,
accrual data, workload, and other research information; present this information at regular research staff
meetings.
" Responsible for timely submission of adverse events, serious adverse events, protocol deviations, and Safety
Letters in accordance with local and federal guidelines.
" Identifies quality and performance improvement opportunities and collaborates with staff in the development
of action plans to improve quality.
" Plans and coordinates strategies for increasing research participant enrollment, and/or improving clinical
research efficiency as needed.
" Provides technical support for the preparation of grant proposals, publications, presentations and special
projects.
" Provides assistance with research project budget development, including identifying and classifying routine
care vs. research related care and provides assistance with research participant research billing and
reconciliation.
Source : Diverse Lynx
