
Healthcare Insurance • Non-profit • Science
Shriners Children's is a non-profit organization that has been providing specialized pediatric care for over 100 years. With a commitment to excellence, their compassionate team of doctors and nurses focuses on delivering personalized care across various specialties, including burn care, orthopedics, and pediatric rehabilitation. They also engage in innovative research aimed at improving medical treatments and the overall quality of life for children.
November 21

Healthcare Insurance • Non-profit • Science
Shriners Children's is a non-profit organization that has been providing specialized pediatric care for over 100 years. With a commitment to excellence, their compassionate team of doctors and nurses focuses on delivering personalized care across various specialties, including burn care, orthopedics, and pediatric rehabilitation. They also engage in innovative research aimed at improving medical treatments and the overall quality of life for children.
• Coordinates and implements SC system-wide processes and initiatives to standardize clinical research operations • Facilitates research activities through collaborative, timely communications with SHC sites and external entities • Maintains and assists with the system wide use and daily operations of the clinical research management system • Accountable for the initiation and maintenance of all Human Subjects and Regulatory documents necessary for submission to SC’s centralized Institutional Review Board • Works with study sponsors and various agencies to obtain initial and continued approval of all clinical trials/clinical research protocols • Demonstrates knowledge of ethical standards set forth by the Belmont Report, the Nuremberg Code and the International Conference of Harmonization GCP standards • Supports coordination of system-wide genomics clinical research activities, including protocol development and executions
• 3 years of clinical research experience (site management, study management, IRB's, and federal regulations regarding clinical research compliance) • Bachelor's Degree in clinical research, science or other healthcare related field - or - 5 years of job-related experience in clinical research administration in lieu of degree • Experience in coordination of intergroup of multi-site clinical studies • Job-related experience in development, review, oversight, or performance management of human clinical studies • Experience with clinical research genomics or strong familiarity with genomics concepts in clinical or research settings • Knowledge of CLIA laboratory sample-processing workflows and foundational genomics terminology • CCRP or CCRC certification • Master's Degree in clinical research, science or other healthcare related field
• Medical coverage on first day! • 403(b) and Roth 403(b) Retirement Saving Plan with matching contributions of up to 6% after one year of service • Paid time off • Life insurance • Short term and long-term disability • Flexible Spending Account (FSA) plans • Health Savings Account (HSA) if a High Deductible Health Plan (HDHP) is elected • Tuition reimbursement • Home & auto insurance • Hospitalization insurance • Critical illness insurance • Pet insurance
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