Clinical Research Coordinator

3 weeks ago

Birmingham, United States Medix Full time

Responsibilities

  • To collect and record preliminary data for clinical research programs
  • To recruit and perform follow-up with research participants as protocols outline
  • To schedule visits according to research protocols
  • To assist in coordination of lab and fieldwork
  • To maintain familiarity with appropriate Good Clinical Practice (GCP) guidelines and regulations
  • Prepares for study monitoring visits
  • Assists with correcting findings
  • Assists with the completion of Case Report Forms (CRF) according to protocol
  • Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance
  • Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials)
  • May perform a variety of medical procedures under supervision
  • May assist in compiling, editing, and proofing written reports for both internal and external administrative offices
  • May perform data analysis using a variety of software packages
  • Uses Electronic Data Capture (EDC) systems necessary for operations under supervision
  • Performs other duties as assigned

Key Duties & Responsibilities

  • Collects and records preliminary data for clinical research programs. Recruits and performs follow-up with research participants as protocols outline. Schedules visits according to research protocols.
  • Assists in coordination of lab and fieldwork. Prepares for study monitoring visits. Assists with correcting findings.
  • Assists with the completion of Case Report Forms (CRF) according to protocol.
  • Assists with development of protocols and standard operating procedures (SOPs) for data quality assurance.
  • Performs general clerical duties (faxing, scanning, routing messages, coordinating the purchase of study supplies/materials).
  • May perform a variety of medical procedures under supervision.
  • May assist in compiling, editing, and proofing written reports for both internal and external administrative offices. May perform data analysis using a variety of software packages.
  • Uses Electronic Data Capture (EDC) systems necessary for operations under supervision
  • Performs other duties as assigned.

Qualifications

  • High School diploma or GED required
  • Prefer candidates with a bachelor's and two (2) years' experience working in a clinical setting
  • Knowledge of clinical trial processes, data collection, data entry
  • Experience with recruiting and performing follow-up with research participants as protocols outline
  • Knowledge of protocols and standard operating procedures (SOPs) for data quality assurance
  • Face-to-face patient communication experience

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