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Banner Health - Phoenix, AZ

posted 2 months ago

Full-time - Entry Level
Phoenix, AZ
Hospitals

About the position

The Clinical Research Coordinator for Orthopedics at Banner Health is responsible for coordinating and implementing clinical research protocols, collecting and recording medical data, assisting in patient assessments, and maintaining study files. This role supports the research efforts of a provider by managing study documentation and ensuring compliance with sponsor-driven timelines, contributing to the advancement of orthopedic care.

Responsibilities

  • Provide study information and obtain relevant information from patients engaged in clinical studies.
  • Assist in the recruitment and screening of volunteers and register patients for clinical trials.
  • Collect and record medical history and relevant medical records data on patients.
  • Explain procedures and consent forms to study participants and compile necessary information prior to initial visits.
  • Respond to inquiries from study participants and update databases with patient information.
  • Perform tasks required by protocol, including obtaining patient medical history, vital signs, and conducting assessments such as phlebotomy and EKG.
  • Triaging adverse events and communicating with the research physician regarding occurrences.
  • Provide educational information to patients and their families, serving as a consistent resource within the clinical research program.
  • Ensure uniform implementation of protocols by completing required documentation accurately and timely.
  • Assist in preparing IRB forms, informed consents, and correspondence with sponsors.
  • Serve as a liaison to other departments and community agencies, ensuring timely communication with referring physicians.
  • May assume primary responsibility for the implementation and management of new clinical trials.

Requirements

  • Bachelor's degree in a healthcare field or equivalent knowledge of clinical research methodologies.
  • 2-4 years of clinical research experience.
  • Familiarity with medical and clinical terminology.
  • Excellent organizational and task management skills.
  • Ability to maintain confidentiality of patient and study information.
  • Knowledge of Federal and State regulations governing clinical practice and research.
  • Strong human relations, organizational, and communication skills.

Nice-to-haves

  • Clinical Research Coordinator Certification (CRCC)
  • Additional related education and/or experience.

Benefits

  • Health insurance coverage
  • Dental insurance coverage
  • Vision insurance coverage
  • 401k retirement savings plan
  • Paid holidays
  • Paid time off
  • Flexible scheduling options
  • Professional development opportunities
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