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Title Data Management Clinical
Target Location US-TX-Plano
Email Available with paid plan
Phone Available with paid plan
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Rahul Goud Veer, Clinical Data ManagerEMAIL AVAILABLE PHONE NUMBER AVAILABLEProfessional Summary Experienced in data management for Phase I, II, and III clinical trials in study set-up, conduct and close out Experienced in handling multiple data sources including labs, imaging, and third-party data sources Skilled in managing data quality and integrity Excellent communication, presentation, and interpersonal skills Effective team player with the ability to manage and work independently to ensure deadlines are achievedProfessional ExperienceTakeda Clinical Data ManagerJan 2023  Present Provide support to clinical data management across clinical programs, enabling planning, coordination, and timely delivery Manage in-house and out-sourced data management activities for ongoing clinical trials Coordinate data Management tasks including protocol review, design of CRFs and edit checks Create and/or review Data management plan, Data transfer agreements and CRF completion guidelines Assist in developing reports, data listing, and trial-specific data specifications for data review Assess the database structures through screen testing and update the database specification for errors Perform and approve User Acceptance Testing to validate the database using standard test scripts Review Case Report Form for consistency and clarity, generate and resolve data queries Support database lock activities as per SOPs and work instructions Therapeutic Expertise Oncology Hematology Cardiovascular Central Nervous Systems Medical DevicesSoftware EDC: Medidata Rave, Oracle Inform,IBL Reporting Tools: J-ReviewSkills MS Word MS Excel (VLookup, Pivot table)Missouri State University Clinical Research Coordinator Sep 2021  Dec 2022 Enter clinical data into both Data Fax and DMS data entry systems. Track entered data in clinical database through 1st pass and 2nd pass data entry Create and generate various reports in conduct, closeout phase for project team review Identify and report the unresolved issues to clinical team which impacts study timelines Perform review of clinical data by patient to identify data trends and data inconsistencies that required further investigation Serve as the query SME for multiple studies Review page verification report, missing pages report and 360 query reports to deliver study status to project team QC clinical data to ensure accuracyHCL Technologies Clinical Data ManagerJan 2019  Aug 2021 Assist in maintenance and closure of study databases Provide study progress updates to Clinical Trial Manager and identifies risks and issues Generate, maintain data management metrics and track query metrics for allocated projects for status updates Assist in design of CRFs, edit checks, CRF completion guidelines and Data transfer agreements Perform User Acceptance Testing (UAT) for developing the eCRFs and edit checks Perform Data Listings review, SAE reconciliation, External vendor reconciliation and issue queries/follow up with external vendors on outstanding issues Utilize listings to identify issues and tracks them until closure to ensure ongoing data cleaning for upcoming deliverables Assess ongoing data review to identify trends, issues with study design and data integrity Prepare, review and analyze reports, and graphs for consistency and accuracy Upload and review the electronic Trial Master File to ensure all data management documents are presentEducation Master of Science in Project Management, Missouri State University, Missouri, USA (2021  2022) Bachelor of Business Management, Osmania University, Telangana, INDIA (2016 to 2019)

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