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Cedars-Sinai · 23 hours ago

Clinical Research Coordinator II - The Angeles Clinic & Research Institute

Los Angeles, CA

Full-time

Onsite

Mid Level

$31.46/hr - $48.76/hr

3+ years exp

Cedars-Sinai is a leader in providing high-quality healthcare and is seeking a Clinical Research Coordinator II to join The Angeles Clinic & Research Institute. This role involves coordinating research studies, ensuring compliance with regulatory requirements, and interacting with various stakeholders to implement research protocols effectively.

CommunitiesHealth CareMedicalNon Profit

Comp. & Benefits

Responsibilities

Establishes and completes 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 growing 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

Participate in meetings and conferences related to research activities, including research staff meetings

Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as vital or requested; Participates in training and education of new research personnel

Qualification

Clinical research coordinationBasic Life Support (BLS)Oncology research experienceSoCRA certificationACRP certificationData collectionPatient recruitmentProject planningQuality improvementTechnical support

Required

Associates Degree/College Diploma required

Basic Life Support Certification (BLS) needs to be the AHA Healthcare Provider Type, required

3 years of clinical research coordination or related experience

Preferred

Bachelor's Degree preferred

SoCRA or ACRP certification preferred

Company

Cedars-Sinai

Glassdoor4.0

Since its beginning in 1902, Cedars-Sinai has evolved to meet the healthcare needs of one of the most diverse regions in the nation, continually setting new standards for quality and innovation in patient care, research, teaching and community service.

Founded in 1902

Los Angeles, California, USA

10001+ employees