Clinical Research Coordinator

You can make a difference in a child’s life. Shriners Children’s is the largest provider of pediatric sub-specialty orthopedic and burn care in Northern California and is recognized by US News and World Report as a top pediatric hospital in the country.

Shriners Children’s is an organization that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience defines us as leaders in pediatric specialty care for our children and their families.

Shriners Children's Northern California offers a competitive salary and benefit package, including medical, dental, vision, disability, retirement, health savings account (HSA), paid time off, pet insurance, continuing education and professional development opportunities. Other considerations include free parking, team-approached interdisciplinary care, friendly environment and the satisfaction that our patients are receiving the best care available.

This is a clinical research position partially funded by a Shriners Hospitals Clinical Outcomes Studies research grant. Funding is subject to annual renewal. This position's primary function is to serve as a Coordinator for the grant(s) funding the position.

This position is full time, non-exempt and health insurance eligible. The pay range for this position is $31.39 - $44.32/hour. Pay is determined based on relevant experience and department equity.

• Provide support and ensure site compliance with the Grant Proposal
• Assemble / process / coordinate approval for The Home Office and local Human Subjects Committees
• Organize and provide training in the use of assessment tools
• Obtain consent from subjects and administer tools at SHCNC
• Maintain ongoing communication between participants, including organizing meetings and facilitating conference calls, to ensure compliance with project deadlines
• Perform chart reviews for eligible patients
• Manuscript development
• Assist in the development of annual progress reports and IRB renewals
• Maintain current knowledge on Federal, local, and institutional clinical research regulatory requirements.
  
  
  

This is not an all-inclusive list of this job’s responsibilities. The incumbent may be required to perform other related duties and participate in special projects as assigned.

Preferred

• 1 year of clinical research experience
• Knowledge of scientific concepts related to the design and analysis of clinical trials
• Ability to prioritize care of patients, aspects of human subject protection, and safety in the conduct of a clinical trial
• Knowledge of how drugs, devices and biologicals are developed and regulated
• Previous experience with study management, safety management and handling of investigational product
• Experience with study and site management, including the financial and personnel aspects
• Understanding of teamwork skills necessary for conducting a clinical trial including all elements of communication within the site and between the site, sponsor and regulators
• Previous experience with how data is acquired and managed during a clinical trial, including source data, data entry, queries, quality control and the concept of a locked database
• Ability to demonstrate leadership and professionalism
• Excellent working knowledge of the Microsoft office suite and verbal and written communication skills.