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Clinical Research Coordinator
Job in
Los Angeles, Los Angeles County, California, 90025, USA
Listed on 2026-01-06
Listing for:
PACER GROUP
Full Time
position Listed on 2026-01-06
Job specializations:
-
Healthcare
Clinical Research, Medical Science -
Research/Development
Clinical Research, Medical Science
Job Description & How to Apply Below
Location: 11800 Wilshire Boulevard Suite 200 & Suite 300, Los Angeles, CA 90025
Shift: Day 5x8-Hour (08:00 - 17:00)
Contract Duration: 13 Weeks
Start Date
: 06/16/2025
Pay Details-
Gross Weekly: XX2,040.00
Taxable Weekly: XX720.00
Non-Taxable Weekly: XX1,320.00
Requirements:
- Associates Degree
- 3+ years of experience as CRC
- 1 year of experience in Oncology
- BLS
- Interest in temp to perm
- Charting: EPIC
- 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.
- Attend meetings and conferences related to research activities, including research staff meetings.
- Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as necessary or requested;
Participates in training and education of new research personnel.
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