August 12, 2016 | By the Resume Genius Team | Reviewed by Mark Slack, CPRW. Job description: Data analyst analyzes and creatively interprets data to provide organizations with effective problem solutions and assist with decision making. Determines correlation between many variables using in-depth statistical software. A data analyst resume example better than 9 out of 10 other resumes. 9,221 Clinical Data Analyst jobs available on Indeed.com. Clinical Data Analyst Resume Sample Work Experience • Assists with the development of guidelines to further the organization’s clinical integration and bundled payment initiatives • Manage and organize; strong problem solving, organizational, and time management skills is required. Responsible for design hypotheses, test and analyze study results, and uses knowledge of State regulatory and accrediting agency requirements to focus data gathering efforts for the organization. RESUME CAPSTONE HCI PROGRAM OUTCOMES Powered by Create your own unique website with customizable templates. Provided Data Management support for clinical trial databases such as: Initial Discrepancy reviews; Discrepancy closeouts; All levels of data QC; Database Listing Reviews August 12, 2016 | By the Resume Genius Team | Reviewed by Mark Slack, CPRW. Average: 5 (5 votes) Written by Maciej Duszyński. Applied query application to obtain a correct and updated Clinical Research Form. Details. How to write a data analyst resume that will land you more interviews. - Choose from 15 Leading Templates. They are responsible for data mining, development, and preparation of data to provide useful information for internal and external stakeholders. How to write Experience Section in Analyst Resume, How to present Skills Section in Analyst Resume, How to write Education Section in Analyst Resume. No need to think about design details. November 29, 2020 resume resume examples [First Name] [Last Name] Contact Address: [street] [Country] [City] [State/Province] [Zip Code] Contact Number: (012)-345-6789. Maintained accurate study documentation and communicated the study status for assigned work. Do you have useful advice on writing resumes for various data analyst positions (clinical data analyst resume or financial data analyst resume)? 9,221 Clinical Data Analyst jobs available on Indeed.com. Validate accuracy, timeliness, and identify/track/support change process, Associate’s degree or equivalent experience, Intermediate Microsoft suite skills (Advanced Excel, Access, PowerPoint skills), 5 years of experience in the Healthcare industry, in a clinic, provider group or health plan setting, 5years in clinical data measurement and outcomes, Extensive experience with coding (ICD, CPT/II, HCPC, etc. Clinical Data Analyst Resume Template in Word. Developed and executed Data Management Plans for multiple protocols simultaneously. Responsible for the development, management, and overall coordination of the CareScience System to facilitate performance improvement and program development within the organization. Specializes at managing and streamlining medical budgets. Reviewed clinical data in the EDC and issue queries as needed. Always prepare before you make a choice. Assist with recruitment and evaluation of clinical analysts, Develop and maintain working relationships with internal UPMC departments, and external contacts as appropriate, Exhibit advanced problem solving using various information sources. After logging in, come back to this page and refresh your browser. Maintains patient confidentiality and ensures data accuracy, Identify trends in outcomes, utilization, medical quality and other areas, Master new computer software programs and upgrades, as applicable, Perform clinical analyses in a team oriented atmosphere and review the analytical outcomes to both clinical and non-clinical audiences, Serve as a role model to the Clinical Data Analyst team, Stay abreast on new solutions relevant to the department through various webinars and intermittent conferences requiring brief trave, Bachelors Degree in Finance, Mathematics, Statistics, Information Systems, Healthcare Management or related field and 5 years experience, MS Office proficiency required SQL/Business Intelligence knowledge preferred, Healthcare experience preferred Excellent interpersonal, oral and written communication skills required, Epic (UPMC's Electronic Medical Record) training is mandatory within the first year of employment, requiring one week of travel to Madison, Wisconsin, Develop critical knowledge of GHI study initiation, execution, analysis and closing procedures; study-related documentation; and study, program and business goals and milestones, Ensure the accurate, complete and timely collection and validation of genomic and clinical data for research studies, Build, configure, and program database structures in a variety of different platforms to maintain and manage genomic and clinical data for research studies, Programmatically manipulate and combine data from a variety of different sources, Work closely with colleagues from Biostatistics, Non-clinical biostatistics, Clinical Operations, Medical, Pathology and Program Management to ensure Data Management needs and status updates are addressed and well-communicated, Interact with collaborators, both internal within Genomic Heatlh and external, in order to gather requirements, plan deliverables and communicate progress and findings, Train clinical site personnel and collaborators on study-specific data management tools, Define and recommend standards, construct datasets and deliver data management oriented analysis and reporting of genomic and clinical data for research studies, Ensure the preparation and maintenance of documentation, as required by departmental standard operating procedures and practices, or regulations, Contribute to the ongoing development and improvement of department infrastructure including work instructions, Standard Operating Procedures and common-use programs, Participate in recruiting and hiring of staff, Train and mentor new and/or lower-level staff, Bachelor’s degree in life sciences, computer sciences, or other relevant discipline, Demonstrated competency with data management processes and procedures, Demonstrated ability to work as the lead data manager/analyst in a project team, Demonstrated programming proficiency with SAS, including moderate to complex data step programming and moderate to complex data reporting, Demonstrated proficiency with relational databases and programming moderate to complex SQL queries, Demonstrated proficiency in software development lifecycle practices including requirements definition, risk assessment and programming validation, Demonstrated coding skills in a modern clinical data management system/EDC platform, including edit check programming and dynamic entry screen programming, Demonstrated competency in the utilization of Microsoft tools, specifically Word; Excel; PowerPoint; and/or Project, Demonstrated excellent oral, written and presentation communication skills, Demonstrated ability to deliver quality results in a timely manner, either independently or by directing others, Demonstrated excellent organization skills and detail orientation, Demonstrated excellent negotiation and conflict resolution skills, Demonstrated ability to be highly effective in a fast-paced, rapid growth environment, Demonstrated programming skills in other data manipulation, analysis and reporting tools such as R and Tableau, Support set-up and testing of data analysis tools, Review clinical and operational study data to identify potential site performance and site organization issues, Train and support the project teams for the use of Clinical Risk Management systems and processes, Manage operational risk log for Clinical Risk management activities, Communicate effectively with the project team, CRAs, Project Managers, Clinical Trial Managers, DM Staff, Medical staff, Scientific Council to ensure decisions are taken to support adequate monitoring intervention and effective resolution of site performance issues, Performs or coordinate all data management activities for assigned studies, as appropriate, Ensures that all data management activities for assigned studies are completed on time and with high quality, Communicates effectively with peers, study teams and management as appropriate to support studies and goals, Leads efforts to improve Data Management processes, as needed/assigned, Represents the Data Management group at study team meetings and cross-functional task forces, Trains and mentors other Clinical Data Associates (CDAs) and Clinical Data Coordinators (CDCs), Applies and promotes best practices and established standards, Serves as a liaison between the study team and clinical data operations, Is a Subject Matter Expert (SME) in most areas within Data Management, Understands the whole clinical trial process and regulations that apply, engages in relevant professional associations or societies, and seeks continuing education about SJM devices and therapies, Suggest and drafts departmental Standard Operating Procedures (SOPs), Departmental Work Instruction (DWIs), and guidelines, Complies with U.S. Food and Drug Administration (FDA) regulations, International Conference on Harmonisation (ICH), ISO 14155, other regulatory requirements, applicable company policies, operating procedures and processes, Master's Degree in Computer Science, Informatics, Health Sciences, related field and a minimum of four plus years’ experience working in a clinical research environment or a Bachelors degree with six plus years’ experience working in a clinical research environment, Experience to include a thorough understanding of clinical data management processes, Strong organizational, project management and risk management skills, as well as attention to detail, Highly skilled with MS Office, especially Excel, Word, Publisher and Powerpoint, Strong ability to work with Clinical Data Management Systems. 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