Clinical Research Coordinator - 236592

job
  • Medix™
Job Summary
Location
Des Moines ,IA 50319
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
21 Nov 2024
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Job Description
  • Collect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.
  • Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.
  • Recruit and screen participants for clinical trials and maintain subject screening logs.
  • Assist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.
  • Maintain source documentation based on protocol requirements.
  • Schedule and execute study visits and perform study procedures.
  • Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.
  • Monitor subject safety and report adverse events/reactions to the Principal Investigator and/or 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, if needed.
  • 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 studies.
  • Performs other duties and projects as assigned.

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