Clinical Research Associate

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.

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 Resarch Associate (CRA) is responsible for verifying that the rights and the well-being of human subjects are protected, and that the reported trial data is accurate, complete, and verifiable from source documents. The CRA ensures that the conduct of the trial complies with the currently approved protocol/amendment(s), with Good Clinical Practice (GCP), and with applicable regulatory requirements. This is a full-time, salaried-exempt position.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

• Oversee site management and clinical monitoring activities in accordance to contractual agreements, department guidelines, SOPs, applicable international, federal and state regulations, as well as IRB guidelines.
• Serves as the point of contact between the sponsor and the investigator.
• Verifies the qualifications and resources of research staff, facilities, and investigational products, ensuring adequacy throughout the duration of the trial.
• Assumes the responsibility for ensuring the safety and proper conduct of the trial.
• Ensures the investigator’s adherence to the approved protocol and all Good Clinical Practice (GCP) procedures.
• Verifies the accuracy, completeness, and maintenance of source data/documents and other trial records.
• Ensures timely and accurate reporting of adverse events, concomitant medications, and intercurrent illnesses in accordance with the protocol and Case Report Forms (CRFs).
• Communicates any deviations from the protocol, SOPs, GCP, and the applicable regulatory requirements to the investigator.
• Other duties as assigned.

SUPERVISORY RESPONSIBILITIES : None.

REQUIRED EDUCATION AND EXPERIENCE:

• Bachelor’s degree or an associate degree in clinical Trials Research related curriculum plus a minimum of one year of healthcare experience.

KNOWLEDGE, SKILLS, AND ABILITIES:

• Must possess superior analytical and creative thinking skills.
• Ability to multi-task and deal with shifting priorities.
• Strong spoken and written communication skills.
• Excellent organizational skills; accurate and detail-oriented.
• Proficient in MS Word and Excel programs.

PHYSICAL DEMANDS AND WORK ENVIRONMENT:

• Frequently required to sit, stand, walk.
• Occasionally required to lift up to 15 pounds at times.

CURE 4 THE KIDS FOUNDATION PARTICIPATES IN E-VERIFICATION.