Clinical Research Coordinator

Marshall UniversityHuntington, WV
13d

About The Position

Job Responsibilities Collaborate with Clinical Activities – PFT , hearing, injections, specimen collection, etc. Clinical support for physician/investigator/clinical team; Ensure clinical findings/reports are communicated timely to proper agency/department; Support various clinical education and training requirements; Shows excellent interpersonal skills to deal effectively with clinicians, patients, administrators, auxiliary personnel, regulators, monitors, and sponsors; Understands and is knowledgeable of medical terminology, good clinical practice, FDA , OHRP , HIPAA policies; Experience with Microsoft Office Suite; Manages workflow independently with excellent organizational skills; Prioritizes quickly and appropriately with the ability to multi-task; Pays meticulous attention to detail Ability to review, understand, and apply complex protocols; Manages study materials including but not limited to, regulatory binders, study specific source documentation protocols training certification and other materials as required.

Requirements

  • Knowledge of medical terminology, good clinical practice, FDA , OHRP , HIPAA policies
  • Experience with Microsoft Office Suite
  • Manage workflow independently with excellent organizational skills
  • Prioritize quickly and appropriately with the ability to multi-task
  • Meticulous attention to detail
  • Ability to review, understand, and apply complex protocols

Responsibilities

  • Collaborate with Clinical Activities – PFT , hearing, injections, specimen collection, etc
  • Clinical support for physician/investigator/clinical team
  • Ensure clinical findings/reports are communicated timely to proper agency/department
  • Support various clinical education and training requirements
  • Effectively deal with clinicians, patients, administrators, auxiliary personnel, regulators, monitors, and sponsors
  • Manage study materials including but not limited to, regulatory binders, study specific source documentation protocols training certification and other materials as required.
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