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Clinical Research Coordinator

Medix Los Angeles Metro Area Full-Time
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  • Job Description:

    • Coordinates with Principal Investigator and school, department, and central administration to help ensure that clinical research and related activities are performed in accordance with federal regulations and university and sponsoring agency policies and procedures.
    • Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to (but not limited to) protocol requirements, schedule of visits, execution of research plan. Maintains documentation of training.
    • Assists Principal Investigator to assure that all key personnel or persons 'engaged' in the research project have met training requirements in accordance with federal regulations and university and sponsoring agency policies and procedures.
    • Cooperates with university compliance and monitoring efforts related to sponsored program administration and reports instances of noncompliance to the appropriate compliance office. Coordinates and facilitates monitoring and auditing visits. Notifies appropriate institutional officials of external audits by FDA and sponsors.
    • Collaborates with PI and institution to respond to any audit findings and implement approved recommendations.
    • Cooperates with university and sponsoring agency compliance and monitoring efforts related to human research participant protection and reports instances of noncompliance to the appropriate compliance office.

    Requirements:

    • Exposure to Research
    • May or may not require a Bachelor's Degree, based on experience
 

Skills required

Pharmaceuticals
Product Quality Assurance
Coordinating
Operations
Leadership
Product Quality Control

Location

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Job ID: 61212

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