Clinical Research Coordinator

Matrix Clinical Research

Clinical Research Coordinator

Los Angeles, CA
Full Time
Paid
  • Responsibilities

    Benefits:

    401(k)

    Competitive salary

    Opportunity for advancement

    Paid time off

    Training & development

    Job Summary

    We are seeking a motivated and detail-oriented Research Coordinator to join our team. The Research Coordinator will play a critical role in supporting our research projects by managing the daily operations, coordinating between different stakeholders, and ensuring the smooth execution of our research studies.

    Responsibilities · Provide clinical research support to investigators to prepare for and execute assigned research studies, including:

    · Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data;

    · Attend all relevant study meetings;

    · Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research;

    · Recruit and screen patients for clinical trials and maintain subject screening logs;

    · Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits;

    · Design and maintain source documentation based on protocol requirements;

    · Schedule and execute study visits and perform study procedures;

    · Collect, record and maintain research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness;

    · Handle lab testing and analysis, including preparation of specimen collection tubes and lab logistics;

    · Monitor subject safety and report adverse reactions to appropriate medical personnel;

    · Correspond with research subjects and troubleshoot study-related questions or issues;

    · Participate in meetings to confirm daily study tasks are assigned to team members and are executed to the expected standards;

    · Assist with study data quality checking and query resolution.

    Qualifications

    Must have Phlebotomy experience

    Must have 3 years as a coordinator

    Spanish Speaking / Bilingual preferred