Cedars-Sinai
Clinical Research Associate I, Per Diem - Castellon-Lopez Lab
Cedars-Sinai, Los Angeles, California, United States, 90079
Job Title:
Clinical Research Associate I, Per Diem - Castellon-Lopez Lab
Company:
Cedars‑Sinai
Required ID:
10495
Base Pay:
$19.50 - $32.86 per hour
Primary Shift:
Day
Shift Duration:
8 hours
Overtime Status:
Non‑exempt
Primary Duties and Responsibilities
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
Provides supervised patient contact or patient contact for long term follow‑up patients only.
Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
Assists with clinical trial budgets.
Assists with patient research billing.
Schedules patients for research visits and research procedures.
Responsible for sample preparation and shipping and maintenance of study supplies and kits.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Maintains research practices using Good Clinical Practice (GCP) guidelines.
Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
Participates in required training and education programs.
Qualifications Requirements:
High School Diploma/GED required.
Preferred:
Bachelor's Degree preferred.
1 year Clinical research related experience preferred.
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Clinical Research Associate I, Per Diem - Castellon-Lopez Lab
Company:
Cedars‑Sinai
Required ID:
10495
Base Pay:
$19.50 - $32.86 per hour
Primary Shift:
Day
Shift Duration:
8 hours
Overtime Status:
Non‑exempt
Primary Duties and Responsibilities
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
Provides supervised patient contact or patient contact for long term follow‑up patients only.
Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
Assists with clinical trial budgets.
Assists with patient research billing.
Schedules patients for research visits and research procedures.
Responsible for sample preparation and shipping and maintenance of study supplies and kits.
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
Maintains research practices using Good Clinical Practice (GCP) guidelines.
Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
Participates in required training and education programs.
Qualifications Requirements:
High School Diploma/GED required.
Preferred:
Bachelor's Degree preferred.
1 year Clinical research related experience preferred.
#J-18808-Ljbffr