Ohio Gastroenterology Group
Research Coordinator
Ohio Gastroenterology Group, Columbus, Ohio, United States, 43224
Job Objective: The Research Coordinator will facilitate all facets of GI clinical research studies.
Duties and Responsibilities: •Administratively and clinically manage industry sponsored clinical trialsAssist with protocol design, where requestedAdhere to Research SOP's, Good Clinical Practices and the study protocolsAssist in patient recruitment by performing detailed chart reviews and patient interviewsDiscuss study protocols with patients and verify the informed consent documentationReview Medical History of patient against Inclusion/Exclusion Criteria of studiesPerform blood draws, process and ship blood/urine specimens per study protocol and IATA regulationsSchedule all patient research visits and procedures consistent with protocol requirementsDispense study medication, collect vital signs and perform ECGsAssist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocolEnsure the filing and maintenance of all regulatory documentsSchedule and prepare for monitor visitsComplete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracyQualifications:
Associates degree in a clinical or scientific related discipline required, Bachelor's degree preferred3+ years previous experience as a clinical research coordinator for pharmaceutical phase II or III trials, GI trials experience preferredComputer skills - Microsoft Word, Excel, Power Point, CTMS, EMRPrevious experience in a role of complex administration or project coordinationEffective communication skills to include written, verbal and presentation skillsStrong attention to detail and organizational, analytical, and problem-solving skillsPeriodic local travel to other practice locations on an as-needed basisPhysical Requirements:
Ability to stand and walk throughout the dayProlonged periods of sitting and performing administrative duties including the use of computersAbility to bend, twist, stoop, and reachAble to lift and carry supplies and equipment as needed (up to 15 pounds)Physical Demands:
Applies the principles of body mechanics in lifting or moving charts, boxes, or equipment (occasional)Must be able to independently lift 25 pounds (occasional)Must be able to sit (frequent), stand (frequent), walk (frequent), stoop (frequent), bend over (frequent), and type on keyboard (frequent).Work Environment:
Medical office requiring some contact with adult patients
Duties and Responsibilities: •Administratively and clinically manage industry sponsored clinical trialsAssist with protocol design, where requestedAdhere to Research SOP's, Good Clinical Practices and the study protocolsAssist in patient recruitment by performing detailed chart reviews and patient interviewsDiscuss study protocols with patients and verify the informed consent documentationReview Medical History of patient against Inclusion/Exclusion Criteria of studiesPerform blood draws, process and ship blood/urine specimens per study protocol and IATA regulationsSchedule all patient research visits and procedures consistent with protocol requirementsDispense study medication, collect vital signs and perform ECGsAssist with routine data verification and quality control, ensuring data integrity and consistency with prescribed study protocolEnsure the filing and maintenance of all regulatory documentsSchedule and prepare for monitor visitsComplete and maintain case report forms per FDA guidelines, and review them against the patient's medical record for completeness and accuracyQualifications:
Associates degree in a clinical or scientific related discipline required, Bachelor's degree preferred3+ years previous experience as a clinical research coordinator for pharmaceutical phase II or III trials, GI trials experience preferredComputer skills - Microsoft Word, Excel, Power Point, CTMS, EMRPrevious experience in a role of complex administration or project coordinationEffective communication skills to include written, verbal and presentation skillsStrong attention to detail and organizational, analytical, and problem-solving skillsPeriodic local travel to other practice locations on an as-needed basisPhysical Requirements:
Ability to stand and walk throughout the dayProlonged periods of sitting and performing administrative duties including the use of computersAbility to bend, twist, stoop, and reachAble to lift and carry supplies and equipment as needed (up to 15 pounds)Physical Demands:
Applies the principles of body mechanics in lifting or moving charts, boxes, or equipment (occasional)Must be able to independently lift 25 pounds (occasional)Must be able to sit (frequent), stand (frequent), walk (frequent), stoop (frequent), bend over (frequent), and type on keyboard (frequent).Work Environment:
Medical office requiring some contact with adult patients