Medical Research Coordinator Lead

2 days ago


Maitland, New South Wales, Australia beBeeClinicalResearch Full time $100,000 - $150,000

K2 Medical Research is a clinical research facility that specializes in conducting multiphasic clinical trials to promote innovative medical treatments while maintaining participant safety and privacy.

Our goal is to fight diseases that affect our loved ones and ourselves by harnessing advanced clinical research and connecting patients with tomorrow's treatments, improving local communities' health.

We seek a skilled professional to support our Maitland clinic. The ideal candidate will manage clinical trials, ensure studies adhere to federal regulations and guidelines, and handle necessary documentation for subject enrollment and maintenance.

Primary Responsibilities:
  • Understand assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigators
  • Ensure strict adherence to study protocols; obtain exemptions when necessary/appropriate
  • Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator
  • Articulate all pertinent issues to the PI or document by email/letter or during meetings
  • Collect initial psychiatric and medical information by interviewing patients and accessing other appropriate sources
  • Ensure communication flow including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitors, Auditors, and any marketing groups hired by the Sponsor
  • Utilize psychiatric rating scales and maintain interrater reliability with other clinicians at K2 Medical Research
  • Perform clinical tasks including vital signs, height and weight, ECG, phlebotomy, specimen packaging
  • Maintain timely source documentation as well as sponsor-required information
  • Dispense and maintain accurate records of study medication
  • Educate patients and family regarding their particular study and clinical drug trials in general
  • Complete monitor and sponsor queries in a timely manner
  • Provide community resource referrals to patients, caretakers, and family at the conclusion of the patient's participation in the study
Key Requirements:
  • HS Diploma or GED required; Bachelor's degree strongly preferred
  • Two years of experience in a clinical environment; experience in clinical research is ideal
  • LPN, RN, or other medical licensure or certification
  • Strong working knowledge of GCP and FDA guidelines
  • Knowledge of medical terminology
  • BLS Healthcare Provider certification required
  • Bilingual in Spanish and English strongly preferred

This role offers an opportunity to work in a dynamic and innovative environment, contributing to the advancement of medical knowledge and treatments.

The successful candidate will possess excellent interpersonal and communication skills, with the ability to work effectively in a team environment.



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