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Clinical Research Coordinator

EmployVisionJefferson City, MO🇺🇸United StatesPosted Sep 22, 2026

Quick Overview

Seniority
Mid Senior
Work mode
Hybrid
Location
Jefferson City, MO, United States
Posted
Yesterday
AuditingClinical ResearchClinical TrialsSchedulingVital Signs

Job Description

  • 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.
  • Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring.
  • Record, report and interpret study findings appropriately to develop a study-specific database.
  • Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.
  • Provide training to new investigator site staff members on study-specific topics and requirements.
  • Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
  • Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
  • Assist research site with coverage planning related to staffing and scheduling for research projects.

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