Clinical Research Liaison Specialist

3 days ago


Scottsdale, Arizona, United States Medix Full time
About the Role

We are seeking a highly skilled and detail-oriented Clinical Research Liaison Specialist to join our team. This is a unique opportunity to contribute to the success of our organization by coordinating research patient visits and ensuring compliance with regulatory requirements.

Key Responsibilities
  • Coordinate daily clinical trial activities, including facilitating sponsor required questionnaires and ensuring study staff is properly trained on study-related information.
  • Manage source documents for each trial, review and comprehend study protocols, and work with the study team to recruit eligible candidates.
  • Collect updated medical history, adverse events, and serious adverse events, and report them to the sponsor and IRB within the required time frame.
  • Conduct and/or participate in the informed consent process, collect data as required by the protocol, and enter information into the electronic data capture system.
  • Oversee data entry, resolve queries, and coordinate monitor site visits.
Requirements

To be successful in this role, you will need:

  • A strong understanding of clinical research principles and regulations.
  • Excellent communication and organizational skills.
  • Ability to work effectively in a team environment.
  • High level of attention to detail and ability to maintain accurate records.
Benefits

This role offers a competitive salary of $65,000 per annum, plus additional benefits, including health insurance, retirement plan, and opportunities for professional growth and development.



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