Clinical Research Coordinator

3 weeks ago


Los Angeles, United States Matrix Clinical Research Full time
Job DescriptionJob DescriptionBenefits:
  • 401(k)
  • Competitive salary
  • Health insurance
  • Paid time off
  • Training & development

Job Summary
Must have 3 consecutive years recent experience in a trial study

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 huddles 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 3 consecutive years recent experience in a trial study
  • Phlebotomy experience / certification preferred
  • Spanish Speaking / Bilingual preferred



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