Clinical Trials Coordinator

2 weeks ago

Los Angeles, California, United States Matrix Clinical Research Full time
Job OverviewBenefits:
  • 401(k) plan
  • Attractive salary package
  • Comprehensive health coverage
  • Career growth opportunities
  • Paid leave
  • Professional training and development

Position Summary
We are looking for a dedicated and detail-focused Clinical Research Coordinator to support our research initiatives. The Coordinator will be essential in overseeing daily operations, facilitating communication among various stakeholders, and ensuring the effective implementation of our clinical studies.

Key Responsibilities
  • Provide essential clinical research assistance to principal investigators in preparing and executing assigned studies, which includes:
  • Reviewing study protocols, Case Report Forms (CRFs), and other specific documentation, along with electronic data capture systems for clinical research data;
  • Participating in all pertinent study meetings;
  • Gathering and submitting regulatory and ethics documentation as mandated by the FDA and other governing bodies;
  • Recruiting and screening participants for clinical trials while maintaining accurate subject screening logs;
  • Informing research participants about the study, including its objectives, procedures, and protocol-related timelines;
  • Creating and managing source documentation in accordance with protocol specifications;
  • Scheduling and conducting study visits and performing necessary study procedures;
  • Collecting, recording, and maintaining research participant data in line with study protocols and standard operating procedures, ensuring quality control for accuracy and completeness;
  • Managing laboratory testing and analysis, including preparation of specimen collection materials and logistics;
  • Monitoring participant safety and reporting any adverse reactions to the appropriate medical personnel;
  • Communicating with research participants to address study-related inquiries or concerns;
  • Participating in meetings to ensure daily study tasks are assigned and executed to the required standards;
  • Assisting with the verification of study data quality and resolving any queries.

Qualifications
  • Phlebotomy experience is required
  • Minimum of 1 year of experience as a coordinator
  • Bilingual candidates, particularly Spanish speakers, are preferred

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