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. Best practices applied to all aspects of CDM project/ study activities, In charge of the development of CRFs, Data Management Plan, Data Validation Plan, Data Review Report as per company standards. Filter by location to see Clinical Data Analyst salaries in your area. Data Analysts are employed in various industries and are responsible for collecting business data, analyzing information, and developing improvement and enhancement solutions based on their findings. Facilitated communication of data management issues to the project team. Works across the organization to provide business process or design recommendations, Supports quality committees and work group in performance improvement efforts, Develop and maintain all clinical databases (e.g., Utilization management, Specialty/Non-Specialty Pipeline, Generic Pipeline, Drug List Management databases), Create and Maintain project documentation relevant to data management activities, Continuously look for ways to streamline and improve the quality of the formulary management process, Contributes to internal process development and improvement, Good interpersonal, verbal and written communication skills, Good analytical skills and attention to detail, Effective time management to meet daily metrics or team objectives, Excellent communication skills, oral, written and presentation, Proficiency in managing and organizing computer files, Bachelor's degree in applied or life science and minimum of 2 years experience in clinical trials (with at least 1.5 years in data management) or equivalent education and work experience, Working knowledge of clinical trials and data management's role in the clinical trials process, Detail-focused for pre-entry review and query management activities, Ability to successfully work on multiple projects and prioritize daily tasks and responsibilities, Effective communications skills both written and verbal, Additional skills might include any of the following: programming in SAS, PL/SQL, analytical capabilities, medical coding (adverse events and medical therapies), 2+ years experience with Qlikview, including development and administration, Proficiency with data input validation techniques and techniques for handling non-standard or variable data, Proficiency with agile software development and systems development life-cycle, Significant experience working with large data sets and numerous data sources to slice and dice for end users to minimize manual effort and deliver a great user experience, Ability to understands and modify any component of QlikView, from Script/model to complex chart creation using set analysis, Must have broad therapeutic area exposure in the clinical development space with the ability to understand and process medical and clinical terminology and data, Must thrive in a fast paced environment with short time frames to deliver reporting with frequently changing requirements, Must have experience with working with several stakeholder groups having input to the output and must be able document and translate requirements into code quickly and accurately, Comprehensive knowledge of all Microsoft Office applications, including Word, Excel, Access and PowerPoint, Previous health insurance industry experience working in a Finance/Accounting department, Prior experience working in a system analytics and/or data warehousing environment is strongly desired, Excellent programming skills desired (SAS, SQL), Excellent PC skills (including MS Word, Excel, PowerPoint, and Access) required, High level proficiency with statistical platforms and reporting tools desired, Degree in Business, Engineering, Mathematics, Statistics, Public Health, Health Care Administration, Accounting or related field desired, Experience in business writing or creative writing desired, Experience with large data sets and/or analysis of health care data is desired, Work with Regional Analysts and Corporate Analysts to enhance warehouse data content, Ability to Identify, Investigate, and Report issues within data systems for resolution, Ability to anticipate future needs and provide the data to support the operations, Work with the clinical areas to develop more automated reports for customer reporting and operational reporting, Develop knowledge of Humana and other clinical programs in order to support these areas through reporting, Working towards degree in Business, Health Administration, Accounting or related field, Independent self-starter requiring minimal supervision, Excellent PC skills (including MS Word, Excel, PowerPoint and Access) required, Must have accessibility to high speed DSL or Cable modem for a home office (Satellite internet service is NOT allowed for this role); and recommended speed for optimal performance from Humana systems if 10Mx1M, Degree in Business, Engineering, Math, Health Administration, Accounting or related field required, Experience with SharePoint Administration, Resides within the Great Lakes Region (MI, IL & WI), Bachelor’s degree and / or other medical qualification or relevant DM experience, Create CRF Completion Guidelines (CCG), SAE reconciliation Guidelines, etc. Performed the tasks of higher level data management activities such as database design and setup, independent review of CDM deliverables, Medical Coding. Work closely with clients to define data and information needs. Flagged sub-studies for possible data entry. Skills : Data Entry Guidelines, Data Warehouse, Data Analysis. Knowledge of medical terminology required. - Instantly download in PDF format or share a custom link. We’d love to hear from you. Samantha Gray. Build My Resume Now Professional Summary Accomplished Clinical Data Associate who has extensive database maintenance and data mining experience. Data Analyst Resume Example. Start your cover letter with a short intro paragraph introducing yourself and detailing the position you are applying for. Download. Performed clinical checks to obtain an accurate and legible Case Report Form by reviewing and correcting using: queries, screening, demographic data, inclusion/exclusion criteria, concomitant medications/dosages, etc. View . Possessing strong technical skills rooted in substantial training as an engineer. Assisted in the resolution of study-related issues by consulting with data managers, project managers, and other team members. Clinical Data Analyst Resume Template in Word. Apply to Data Analyst, Data Scientist, Research Assistant and more! Adept at multi-tasking and managing time efficiently. Download. 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. You have a very intelligent data analyst resume here that shows how a proper resume objective should be written. Objective : Highly dependable and personable Clinical Data Analyst Professional with over five years of experience in cash management, advanced clerical procedures, and organization operations within the medical and customer service industries. Work closely with business users and application team to design, build and execute a user acceptance test plan, Prepares report management documentation to manage reports library, track project progress and reports problems in a timely fashion. Review study data accurately to identify site performance issues, Communicate effectively with the project team, CRAs, DM Staff, Medical staff, Scientific Council to ensure adequate monitoring intervention and effective resolution of site performance issues, Work with Data Management, Clinical Operations, Central Laboratory, ITG, Biostatistics, Medical Writing, Regulatory Affairs and Quality Assurance to ensure all data collected within a clinical study are managed according to corporate standards and meet regulatory guidelines for data integrity, Bachelor’s degree or local equivalent in a scientific discipline and/or appropriate experience, Knowledge of regulatory requirements respecting data quality and clinical trials conduct, Must possess excellent oral communication skills and attentiveness to detail, Proven leadership skills and the ability to work independently to resolve study related issues, Ability to work within a team environment and manage competing priorities in a changeable environment, Knowledge of database technologies and processes, Ability to handle stressful situations and deadlines, Manage projects working with customer data managers and internal team members to ensure protocol adherence, workload projections, and provide technical expertise. Example resumes for this position indicate skills like determining the needs, requirements, and optimization of defined clinical applications in the acute and ambulatory areas; participating in the testing, implementation and support of new application code … Issued data clarification forms to study sites to correct erroneous, incomplete, or implausible data. Clinical data analyst jobs are expected to become more common as the use of digital medical records increases. Clinical Oracle is preferred, Certified Clinical Data Manager (CCDM) preferred, Understands databases; good technical skills in querying and analyzing data (SQL, SAS preferred or equivalent), Experience working in a broader enterprise/cross-division business unit model preferred, Exhibit advanced problem solving using various information sources, Interact with various clinical and non-clinical teams throughout each project to ensure data definitions and assumptions are accurate, Maintain high level of accuracy and timeliness, Maintains patient confidentiality and ensures data accuracy, Bachelors Degree in Finance, Mathematics, Statistics, Information Systems, Healthcare Management or related field and 4 years experience, MS Office proficiency required SQL/Business Intelligence knowledge preferred Healthcare experience preferred, Excellent interpersonal, oral and written communication skills required, Must work well independently and within a team, Technical expertise in use of data management tools, Ability to work collaboratively with sites and project teams to deliver a clean database, Ability to anticipate data quality issues during design and planning stages, Ability to offer solutions to data handling issues, Ability to overcome obstacles and consistently meet deadlines, Ability to lead a team of CDAs on assigned project(s), 2 or more years demonstrated success in leading a data quality review team, Work with senior management, technical and client teams in order to determine data requirements, business data implementation approaches, best practices for advanced data manipulation, storage and analysis strategies, Write and code logical and physical database descriptions and specify identifiers of database to management system or direct others in coding descriptions, Support development of DM study documentation, including: Data Management Plans, annotated CRFs and specifications, CRF Completion Guidelines, Data Transfer Plans, etc. Completes assigned tasks as defined by project timeline, Trains end-users in reporting database(s) and ad-hoc report creation. Maintains knowledge of current regulations and technologies related to the data management function, Participates in the implementation of department initiatives, Assume the mentor role for junior staff and oversee the quality of data management activities for designated mentee, Analyzes, interprets, and understands data as well as how it supports a business case on operational performance with quality performance metrics involving physicians, Understands and can create health system, function and department-level peer groups, as well as, compare/benchmark peer groups based on units of service and other adjustment factors, Collaborates and provides data analytics support to the Health System and the ministries, Works with team of analysts in complex data gathering and analytic projects against tight timelines, When requested, attends meetings and creates data presentations and slides as requested to support and answer questions from data owners, Assists with the development of guidelines to further the organization’s clinical integration and bundled payment initiatives, Coordinates daily operations of CHP, including contract management and physician inquiries, Works with Crimson software and Dedicated Advisor to load and collect data from the Crimson database, Generates timely reports for Project Specialist and Director and corresponding physician committees using Crimson software to provide statistical evidence and performance tracking, Exercises creative approaches to problem solving. Support and maintain documentation and training for clinical analytics and reporting libraries, Provides oversight and guidance in the resolution of complex reporting and analytics issues utilizing available resources and expertise in support of reporting and analytic objectives, Interface and serve as liaison with development and deployment teams to provide analytical insights applicable to current program management as well as future program development, 3+ years’ experience in healthcare financial data analysis, and / or medication process analysis, translating analytic concepts, approaches, and results. Develop and modify reporting configurations that meet design requirements. 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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