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The Patient Cloud Data Analyst is a key player in protecting the health of a study from a data perspective. This position possesses a solid clinical data management experience with a focus on applying data analysis to enable ongoing data cleaning activities leading to the on-time delivery of high-quality Clinical outcomes.
Support planning and conduct of eCOA clinical studies across the phases (I-IV)
Provide solid Data Management support and guidance during decision making and/or issue resolution process
Contribute to cross-functional expectations on data quality and data cleaning activities incorporated into the Data Management Quality Plan
Adhere to industry data collection and handling standards to ensure consistency and facilitate downstream processing (e.g., QC testing)
Design and develop QC checks to support ongoing data cleaning to identify issues/risks in data quality and data cleaning performance
Support and maintain strong alliances cross functionally with internal teams
Discuss and design project specific technical solutions which support the data management quality plan
Continuously improve Data Management service processes and data quality measures
Deliver high quality Clean Data
Contributes to a transparent benchmarking of Data Management activities within function and study team
Initiates the DTS package and contributes to the set-up and testing of the eCRF incl. Edit Checks, data listings, and reports, in close cooperation with study team
Your Competencies:
Industry knowledge of Clinical Trial processes, specifically as they relate to eCOA data collection, Data Management Quality Plans (DMQP), standards, management, and preparation for statistical analysis
Experience in study planning and optimization, and knowledge across eCOA clinical development practice areas/technologies as a whole
Experience with Data Analysis, and applying critical thinking to solve problems
Positive attitude and team player
Ability to absorb and apply new information quickly
Ability to think logically to solve complex problems
Solid analytical and technical skills with regard to software applications
Strong collaboration and team-building skills
Excellent verbal and written communication skills
Strong organizational and time management skills
Self-motivated, able to assume responsibility and work autonomously in a professional manner
Experience in developing of Standard Operating Procedures
Adaptable to changing business needs and/or product landscapes
Experience in Medidata RAVE
An exposure to data visualization tools and complex data bases would be a plus
Your Education & Experience:
Minimum 4-year university/college degree with 3+ years of clinical data analysis experience
Experience working with clinical trials, or equivalent combination of education and experience required.
Prior services delivery experience required
Experience supporting project teams and meeting project timelines
Prior data management or clinical trial software consulting experience preferred
