Clinical Research Administrator

2 weeks ago

Kingman, United States Kingman Regional Medical Center Full time
Unlock your potential for professional development We are hiring a full time Clinical Trials Research Administrator at our Cancer Center This position is onsite Located in northwest Arizona, Kingman has a mild climate with stunning Arizona sunsets In the shadows of beautiful mountain ranges and nearby lakes, Kingman is an outdoor enthusiasts' paradise with abundant sunshine and is a great community to live, work and play Benefits (Full Time Employees) We offer you an excellent total compensation package, including a competitive salary, comprehensive benefits, and growth opportunities:
  • Exceptional Colleagues
    • Join us and you'll be a part of a culture where we support each other and celebrate what makes each of us a special person as we work together with integrity, compassion, teamwork, respect, and accountability.
    • Our leaders demonstrate their commitment by gathering feedback, supporting, and empowering team members to do their best work through regular leadership rounding.
  • Health and Well-Being
    • Medical, Dental, Vision, Employer Paid HSA for HDHP participants, Robust Wellness and Employee Assistance Program, Employer Paid Group Life, Short & Long-Term Disability
    • Generous Paid Leave Accruals
    • 403b Retirement Plan with Employer Contributions
    • Employee Recognition Programs, Employee Discounts, and Employee Referral Bonus Program
    • Employee Identity Theft Protection
    • On-site daycare exclusive to our employees children of all ages
    • Employer Paid Employee Wellness Center Membership with fitness classes, personal training, indoor pool, racquetball, and basketball courts
  • Career Growth and Development
    • Tuition Reimbursement/Scholarships for full-time employees
    • As a not-for-profit organization, our employees who have qualified student loans may be eligible for the Public Service Loan Forgiveness program
    • So much more
Position Purpose All KHI employees are expected to perform their respective tasks and duties in such a way that supports KHI s
vision to be among the kindest, highest quality health systems in the country.
The Clinical Research Administrator will design, coordinate, and oversee research projects and the clinical
trials program within the Cancer Center department. Key Responsibilities • Works with director and medical director to formulate the oncology clinical trials accrual plan.
• Adheres to the oncology clinical trials accrual plan.
• Recruits and enrolls study participants.
• Opens and closes clinical trials at the study site with the approval of the director, medical director and
KHI IRB.
• Inputs clinical research data into electronic data systems.
• Coordinates patient visits and procedures related to research.
• Acts as resource for study participants by answering questions and explaining related procedures.
• Ensures the study site follows all local and federal laws and regulations.
• Monitors study sites and activities to ensure the appropriate industry protocols and terms of the study
are being followed.
• Creates thorough documentation of study protocol and updates as needed.
• Provides oversight to the research in the Cancer Center.
• Provides analytic/statistical support as needed.
• Ensures facility maintains adherence to the American College of Surgeon s Commission on Cancer s
research standards.
• Oversees accuracy and timeliness of billing charges related to clinical trials.
• Ensures all staff have adequate training and certifications to treat patients in clinical trials Required Qualifications
  • Experience: 2+ years of research experience or 5 years of clinical experience.
  • Education: Bachelor s degree in nursing or bachelor s degree in a related field.
  • Certification/Licensure: Certificate of Completion from Collaborative Institutional Training Initiative (CITI) Program within 6 months of hire.

Knowledge, Skills and Abilities:
• Must be proficient in basic computing software including but not limited to Microsoft Word, Excel,
Power Point and Outlook.
• Must possess the ability to write both scientifically and analytically.
• Must be proficient in statistical analysis Preferred Qualifications
• Master s Degree in nursing or research related field.
• Certified Clinical Research Associate or Clinical Research Coordinator Credentials.
• Principal Investigator Credentials.

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