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Clinical Research Associate

4 months ago


Las Vegas, United States Cure 4 Full time
We don't train our people to be nice... We simply hire nice people

We are looking for the brightest and the best to join our team

Two major benefits offered by Cure 4 The Kids Foundation
  • One of the most competitive compensation and comprehensive benefit packages in the field of healthcare
  • A state-of-the-art clinical and administrative environment located at 215 and Town Center, Summerlin on the Roseman University Campus
Cure 4 The Kids Foundation was voted #10 on the list of the Best Non-Profits to Work For in the U.S.

If you instinctively say yes to the following questions, this may be your next career opportunity:
  • Are you an exceptional Health Information Supervisor who absolutely thrives on getting things done with a high level of accuracy while being part of an accountable team?
  • Can you be relied upon to be proactive in collaborating with others to solve problems in real-time for our physicians?
WHAT IT TAKES TO BE PART OF OUR TEAM
Are you an exceptional Clinical Research Associate who absolutely thrives on being an integral part of a collaborative and accountable team serving the needs of children and their families? Do you bring the highest standards of integrity and professionalism to your team? Do you thrive in an environment where you are valued and appreciated for who you are, how hard you work and for that something special you bring to the teams you choose to work with? Are you looking for an organization that offers competitive compensation and one of the broadest and most comprehensive benefit packages available in the field of healthcare?

If you said yes to all of these questions and feel you can add to our culture, please keep reading…

Our research team play a vital role that requires a multi-disciplinary team approach to solving problems and patient challenges. "That's not my job" or "someone else can do it" is not in our team vocabulary because we are here to be of support to each other.

SUMMARY:The Clinical Research Associate has an important task within the clinical trial process. He or she has the responsibility to verify that the rights and well-being of human subjects are protected and that the reported trial data is accurate, complete, and verifiable from source documents. Most importantly, the CRA makes sure that the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP, and with applicable regulatory requirements. This is an exempt position.

ESSENTIAL DUTIES AND RESPONSIBILITIES:
  • Responsible for site management and clinical monitoring in accordance with contractual agreements, department guidelines, SOP’s, applicable international, federal and state regulations and IRB guidelines.
  • Act as the main line of communication between the sponsor and the investigator.
  • Verifying that all research staff, facilities and investigational products have adequate qualifications and resources and these remain adequate throughout.
  • Responsible for the safety and proper conduct throughout the trial.
  • Verifies that the investigator follows the approved protocol and all GCP procedures.
  • Verifies that source data/documents and other trial records are accurate, complete, and maintained.
  • Adverse events, concomitant medications, and intercurrent illnesses are reported in accordance with the protocol on the CRFs.
  • Communicates deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator.
  • Performs other related duties incidental to the work described herein.
KNOWLEDGE, SKILLS, AND ABILITIES:
  • Must possess superior analytical and creative thinking skills
  • Excellent attention to detail and the ability to keep detailed, accurate records
  • Strong written and verbal communication skills
  • Advanced organizational and planning skills
  • Proficiency in MS Word and Excel programs

EDUCATION and/or EXPERIENCE:
Completion of an allied health degree (e.g., Respiratory Therapy, Radiology Technology, and Licensed Practical Nurse) or an Associate’s degree in Clinical Trials Research related curriculum plus a minimum of one year of healthcare experience preferred.

PHYSICAL DEMANDS:
Requires sitting and standing associated with a normal office environment. Manual dexterity needed for using a calculator and computer keyboard. This description is intended to provide only basic guidelines for meeting job requirements. Responsibilities, skills and working conditions may change as needs evolve.

SUPERVISORY RESPONSIBILITIES: None.

LANGUAGE SKILLS: Spanish speaking preferred, but not required

CURE 4 THE KIDS FOUNDATION PARTICIPATES IN E-VERIFICATION.