About The Position

Up To $25,000 Sign On Bonus For Qualified RNs! Position Summary: Coordinate multiple in‐patient and out‐patient clinical research protocols. This coordination requires extensive knowledge for the disease pathophysiology, pharmacology treatments, patient disease evaluation workflow, and the ability to collaborate and communicate new processes related to research with the involved departments.

Requirements

  • Must have Registered Nurse license in state in which working and meet one of the following: 1. Five years clinical experience in a healthcare setting, or 2. Bachelor of Science degree with 3 years full time nursing experience or 3. Certification as a Clinical Research professional
  • Three years full time experience in the nursing field required.
  • Experience successfully leading or advancing a project with peers, leadership, and/or external customers.

Nice To Haves

  • Desire certification in the disease specialty being studied or as a Clinical Research Professional.

Responsibilities

  • Coordinate individual clinical research projects in multiple disease conditions.
  • Collaborate with the manager and executive director for the development of department research programs.
  • Coordinate the study protocol procedure events and treatment planning with the investigator.
  • Administering and dispensing investigational medication ordered for that patient by a licensed physician in the dosage prescribed by protocol.
  • Retrieval of medication and assessment of compliance by patient to the protocol.
  • Collaborate with director, manager, research team members and IRB coordinator in developing and revising process flow for research procedures.
  • Assist physicians in protocol development.
  • Advise department manager on resource utilization and training needs.
  • Perform other duties as assigned by the director or manager.
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