
10,000+ employees
🧬 Biotechnology
🔬 Science
🤝 Non-profit
💰 $5.4M Grant - City of Hope on 2024-05
Biotechnology • Science • Non-profit
City of Hope is a nonprofit, NCI-designated comprehensive cancer center and research hospital near Los Angeles that provides patient care, conducts translational biomedical research, and offers education and clinical trials across a national network. It focuses on cancer, diabetes, and other life‑threatening diseases, combining clinical services, laboratory science, training and community outreach to develop new treatments and support patients and families.
🕒 June 20
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10,000+ employees
🧬 Biotechnology
🔬 Science
🤝 Non-profit
💰 $5.4M Grant - City of Hope on 2024-05
Biotechnology • Science • Non-profit
City of Hope is a nonprofit, NCI-designated comprehensive cancer center and research hospital near Los Angeles that provides patient care, conducts translational biomedical research, and offers education and clinical trials across a national network. It focuses on cancer, diabetes, and other life‑threatening diseases, combining clinical services, laboratory science, training and community outreach to develop new treatments and support patients and families.
• Support a vast portfolio of City of Hope therapeutic investigator-initiated studies that require data capture in a robust database. • Work directly with study teams to understand specific workflows and requirements and build electronic Case Report Forms (eCRFs). • Provide programming of validation checks and custom functions on eCRFs to improve data quality. • Develop specifications for standard edit checks, data listings and reports as needed. • Create documentation related to requirements, user testing, and findings. • Provide end user support; communicate with participating sites on data related tasks. • Maintain documentation of all programs and applications. • Support research, evaluation and development of departmental initiatives and new technologies/innovations to improve processes.
• Bachelor degree in Science, Engineering, or Public Health. • A minimum of 5 years’ experience in healthcare / clinical research setting. • Experience in form design and programming in an EDC, such as Medidata Rave, Oracle InForm and/or Forte Oncore / EDC, highly desired. • Experience in clinical research operations, protocol development, and/or research coordinator a plus. • Medidata Rave Study Builder Training, Forte EDC Study Builder Training 5+ years of experience in healthcare / clinical research setting. • Ability to analyze complex clinical trial protocols and refine language into an external system. • Must have the ability to work closely and effectively with a diverse group of administrators. • Must have a passion for excellent customer service and commitment to exceptional quality.
• Comprehensive Benefits
Apply Now🕒 June 20
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💰 $275k Venture Round on 2010-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧐 Analyst
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