Clinical Non-Licensed Pool/Clinical Research Coordinator - Diverse Linx
Los Angeles, CA
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 Linx
