Clinical Research Administrator

3 weeks ago

Kingman, United States Kingman Regional Medical Center Full time
Job Description

Unlock your potential for professional development We are hiring a full time Clinical Trials Oncology RN or 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
Key Responsibilities [List of material responsibilities and essentials duties which must be completed in achieving the objectives of the position]
  • 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.
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 fromCollaborative 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.
Preferences
  • 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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