Clinical Research Coordinator

Conifer Health SolutionsPhoenix, AZ

About The Position

Responsible for coordinating clinical research projects and/or trials at Abrazo Medical Group, Abrazo Central/ Scottsdale Campus and Abrazo West Campus and other Abrazo facilities if necessary; also, able to perform any other research related activities as required.

Requirements

  • Education: High School Diploma and Bachelor’s Degree or relevant professional experience.
  • Experience: Must have a minimum of five years of clinical experience working in a physician office or five years administrative experience; must have a minimum of two years working in a research capacity
  • Other Requirements: None

Nice To Haves

  • Certification : Nursing degree is preferred but not required; ACRP clinical research certification is preferred.
  • Current CITI training, BLS is preferred.

Responsibilities

  • Adheres to and supports the mission, purpose, philosophy, objectives, policies, and procedures of Tenet Physician Resources.
  • Adheres to the Tenet HIPAA Compliance Plan and the Privacy Standards Confidentiality Agreement.
  • Demonstrates support for the Tenet Corporate Compliance Program by being knowledgeable of compliance responsibilities as expressed in the Code of Conduct; adhering to federal and state laws, rules, regulations, and corporate policies and procedures policies that affect his/her specific job functions/responsibilities; and reporting compliance issues/concerns in a timely and appropriate manner.
  • Be knowledgeable of protocols and adhere to Tenet Clinical and Administrative Standards of Practice
  • Meet with Sponsors, Groups, Hospital officials, PIs and ancillary staff prior to study initiation.
  • Maintain ongoing oversight of study project activities, status and timeliness.
  • Interface with research director, PIs and research committee (FRCs)
  • Responsible for creating the FRC agenda, sending the invite, presenting the research projects on the agenda to the FRC members, writing the minutes and notify the PIs of the voting result
  • Attend research meetings, staff meetings, PI meetings, monitor meetings, conference calls.
  • Attend FDA and monitor audits.
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