Clinical Research Coordinator - Cardiothoracic Surgery - Sponsored Research

ProMedica

Toledo, OHFull-time

Behavioral Health Market Context

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Job Description

mer service skills and the ability to work in a fast-paced environment are a must. In addition, for 15 consecutive years, residents of Greater Toledo have named us the Consumer Choice Award winner in our market. In fact, we’re the only hospital in northwest Ohio to receive this honor.

The Clinical Research Coordinator/ CRC coordinates cardiothoracic surgery-focused study protocols for the ProMedica research department. Clinical trials involve enrolling patients in device, medication and registry trials related to all areas of cardiothoracic surgery such as valve replacement and investigational medications for anticoagulation, renal failure and low cardiac output. Performs necessary patient procedures and data collection to ensure compliance with Federal and local research regulations. Maintains all documents in regulatory binder. Maintains patient-specific documentation and enters data into case report forms. Maintains thorough knowledge of all protocols. Ensures all documentation is complete.
Job Requirements
• RN with valid license given priority
• Due to complex nature of tasks and extent of written and verbal communication, Science degree or degree in Health related field preferred.

The above list of accountabilities is intended to describe the general nature and level of work performed by the incumbent; it should not be considered exhaustive.

ProMedica

Qualifications

  • Excellent customer service skills and the ability to work in a fast-paced environment are a must
  • RN with valid license given priority

Benefits

    Responsibilities

    • Clinical trials involve enrolling patients in device, medication and registry trials related to all areas of cardiothoracic surgery such as valve replacement and investigational medications for anticoagulation, renal failure and low cardiac output
    • Performs necessary patient procedures and data collection to ensure compliance with Federal and local research regulations
    • Maintains all documents in regulatory binder
    • Maintains patient-specific documentation and enters data into case report forms
    • Maintains thorough knowledge of all protocols
    • Ensures all documentation is complete


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