Clinical Research Management Analyst job in San Francisco, CA| Recruit Arrow
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Clinical Research Management Analyst
Location : California, San Francisco
Refer job # NYMW338144
Job Responsibilities and Requirements: The individual will manage incoming requests for new protocols and amendments, and ensure the end-user requests are handled in a timely and professional fashion as directed. This may require meeting with UCSF faculty and staff to ensure their research project is reflected accurately in the system and explain any system settings that may impact the system configuration. Applies acquired skills and professional clinical applications concepts for small to medium sized projects of moderate scope. Operates independently within defined scope of responsibilities. Required Qualifications Bachelor's degree in health care information technology, computer science, or related area, and one to three years of relevant experience, and / or an equivalent combination of experience / training Working knowledge of clinical applications systems and functions, including development, implementation, user support, maintenance, and system testing and evaluation Working knowledge of departmental systems and procedures for documentation and reporting, with the ability to perform tests, and to analyze, and interpret relevant data Experience assessing clinical research protocols Knowledge of data standards best practices in research and healthcare, scientific, and medical concepts and terminology Demonstrated knowledge of confidential HIPAA policies as they relate to clinical research and electronic databases Prior experience in a healthcare environment of clinical research setting Demonstrated skills in written and verbal communications, with the ability to convey technical information to clinical users in a clear and concise manner Demonstrated problem-solving skills, with the ability to quickly diagnose problems and develop multiple options for effective and timely resolution of issues and problems Demonstrated interpersonal and customer-service skills to collaborate productively on a team and to provide training and support to clinical providers and staff Detail oriented, with demonstrated organizational skills and the ability to manage time efficiently, prioritize tasks, set schedules, and complete projects in a timely and cost-effective manner Excellent customer responsiveness in all end-user interactions Note: Fingerprinting and background check required. Preferred Qualifications Prior experience as a Clinical Research Coordinator Extensive knowledge of study design criteria and data collection strategies Knowledge of coverage analysis, medical billing terms and research billing operations for industry-sponsored studies License/Certification n/a.
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