PACER GROUP
Job description:
Position: Clinical Research Coordinator
Facility: Cedars-Sinai Medical Center
Location: Los Angeles, CA 90025
Shift: Day (5x8 Hours),8:00 17:00, 40 hours/week
Assignment length: 13 weeks, onsite position (No hybrid role)
Start Date:-11/24/2025
Requirements:
- Bachelor's degree required
- 5 years of experience in clinical research
- 5 years of experience in IRB clinical research application procedures.
- 5 years of experience in Phase I, II, III, IV clinical trials (robust portfolio)
- Experience with protocol writing and investigator-initiated trials
Primary Duties and Responsibilities:
- Provides clinical research expertise by participating in the design and implementation of research projects and care of research patients as needed by the department or institution.
- Responsible for specific and assigned aspects of research infrastructure development and/or maintenance.
- Coordinates research projects at an institutional or departmental level. Serves as an internal consultant for specific departmental activities.
- Communicates project status and improvement areas with leadership in a timely manner. Projects may include but are not limited to investigator-initiated protocol development including protocol writing, case report form development, budget development, and coordination of departmental research committees.
- Implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts.
- Provides guidance regarding project planning, project logistics, and project implementation
- Participates in required training and education programs. Participates in weekly research staff meetings.
- Provides clinical expertise and support with quality assurance, performance improvement, and health plan compliance for clinical trial compliance.
- Ensures the completion and maintenance of consent forms, case report forms, SAE's and source documents to ensure that research is being conducted according to FDA, HSPC, HIPAA and other agency guidelines.
- Completes appropriate IRB paperwork and submission/filing of internal and external SAEs to IRB. Responsible for insuring timely submission of complete, accurate and neat documents to research sponsors, IRB, and contract research organizations, where applicable.
- Acts as a liaison with Principal Investigators, pharmaceutical company representatives and other project funding organizations to monitor and update project progress.
- Prepares for institutional, pharmaceutical and internal audits, including facilitating third party study monitoring.
- Attends site feasibility visits and site initiation visits for potential studies and assures that new studies are implemented according to protocol.
- Review pertinent medical records to determine opportunities for quality improvement. Analyze quality metric data in support of the Principal Investigator and Director of Clinical Services. Recommend and implement process improvement efforts.
- Assists with procedures and supports related patient care when required during data collection process.
Position: Clinical Research Coordinator
Facility: Cedars-Sinai Medical Center
Location: Los Angeles, CA 90025
Shift: Day (5x8 Hours),8:00 17:00, 40 hours/week
Assignment length: 13 weeks, onsite position (No hybrid role)
Start Date:-11/24/2025
Requirements:
- Bachelor's degree required
- 5 years of experience in clinical research
- 5 years of experience in IRB clinical research application procedures.
- 5 years of experience in Phase I, II, III, IV clinical trials (robust portfolio)
- Experience with protocol writing and investigator-initiated trials
Primary Duties and Responsibilities:
- Provides clinical research expertise by participating in the design and implementation of research projects and care of research patients as needed by the department or institution.
- Responsible for specific and assigned aspects of research infrastructure development and/or maintenance.
- Coordinates research projects at an institutional or departmental level. Serves as an internal consultant for specific departmental activities.
- Communicates project status and improvement areas with leadership in a timely manner. Projects may include but are not limited to investigator-initiated protocol development including protocol writing, case report form development, budget development, and coordination of departmental research committees.
- Implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts.
- Provides guidance regarding project planning, project logistics, and project implementation
- Participates in required training and education programs. Participates in weekly research staff meetings.
- Provides clinical expertise and support with quality assurance, performance improvement, and health plan compliance for clinical trial compliance.
- Ensures the completion and maintenance of consent forms, case report forms, SAE's and source documents to ensure that research is being conducted according to FDA, HSPC, HIPAA and other agency guidelines.
- Completes appropriate IRB paperwork and submission/filing of internal and external SAEs to IRB. Responsible for insuring timely submission of complete, accurate and neat documents to research sponsors, IRB, and contract research organizations, where applicable.
- Acts as a liaison with Principal Investigators, pharmaceutical company representatives and other project funding organizations to monitor and update project progress.
- Prepares for institutional, pharmaceutical and internal audits, including facilitating third party study monitoring.
- Attends site feasibility visits and site initiation visits for potential studies and assures that new studies are implemented according to protocol.
- Review pertinent medical records to determine opportunities for quality improvement. Analyze quality metric data in support of the Principal Investigator and Director of Clinical Services. Recommend and implement process improvement efforts.
- Assists with procedures and supports related patient care when required during data collection process.